UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25245349_25245354dup | CA645572123 | KRAS | c.32_37dup (p.Gly12_Gly13insAlaGly) c.-88+5398_-88+5403dup (n.-88+5398_-88+5403dup) | COSMIC |
| 12 | g.25245353_25245358dup | CA645572134 | KRAS | c.30_35dup (p.Gly12_Gly13insAlaGly) c.-88+5396_-88+5401dup (n.-88+5396_-88+5401dup) | COSMIC COSMIC COSMIC |
| 12 | g.25245350_25245360delinsTCAGCTCCAAA | CA891842143 | KRAS | c.25_35delinsTTTGGAGCTGA (p.Val9_Gly12delinsPheGlyAlaAsp) c.-88+5391_-88+5401delinsTTTGGAGCTGA (n.-88+5391_-88+5401delinsTTTGGAGCTGA) | |
| 12 | g.25245351_25245353delinsAAA | CA645572140 | KRAS | c.32_34delinsTTT (p.Ala11_Gly12delinsValCys) c.-88+5398_-88+5400delinsTTT (n.-88+5398_-88+5400delinsTTT) | COSMIC |
| 12 | g.25245353G>A | CA384157465 | KRAS | c.32C>T (p.Ala11Val) c.-88+5398C>T (n.-88+5398C>T) | dbSNP COSMIC |
| 12 | g.25245353G>C | CA384157466 | KRAS | c.32C>G (p.Ala11Gly) c.-88+5398C>G (n.-88+5398C>G) | dbSNP |
| 12 | g.25245353G= | CA2022898472 | KRAS | c.32C= (p.Ala11=) c.-88+5398C= (n.-88+5398C=) | |
| 12 | g.25245353G>T | CA384157463 | KRAS | c.32C>A (p.Ala11Asp) c.-88+5398C>A (n.-88+5398C>A) | gnomAD v4 |
| 12 | g.25245353_25245354insGCC | CA16619504 | KRAS | c.31_32insGGC (p.Ala11delinsGlyPro) c.-88+5397_-88+5398insGGC (n.-88+5397_-88+5398insGGC) | ClinVar dbSNP |
| 12 | g.25245354C>A | CA384157468 | KRAS | c.31G>T (p.Ala11Ser) c.-88+5397G>T (n.-88+5397G>T) | ClinVar |
| 12 | g.25245354C>G | CA384157470 | KRAS | c.31G>C (p.Ala11Pro) c.-88+5397G>C (n.-88+5397G>C) | COSMIC |
| 12 | g.25245354C>T | CA384157471 | KRAS | c.31G>A (p.Ala11Thr) c.-88+5397G>A (n.-88+5397G>A) | COSMIC COSMIC |
| 12 | g.25245355_25245357dup | CA645572142 | KRAS | c.29_31dup (p.Gly10_Ala11insGly) c.-88+5395_-88+5397dup (n.-88+5395_-88+5397dup) | COSMIC COSMIC COSMIC |
| 12 | g.25245355_25245357del | CA2580085331 | KRAS | c.29_31del (p.Gly10del) c.-88+5395_-88+5397del (n.-88+5395_-88+5397del) | ClinVar |
| 12 | g.25245356_25245361dup | CA891842147 | KRAS | c.26_31dup (p.Gly10_Ala11insValGly) c.-88+5392_-88+5397dup (n.-88+5392_-88+5397dup) | |
| 12 | g.25245355T>A | CA478892011 | KRAS | c.30A>T (p.Gly10=) c.-88+5396A>T (n.-88+5396A>T) | |
| 12 | g.25245355T>C | CA478892012 | KRAS | c.30A>G (p.Gly10=) c.-88+5396A>G (n.-88+5396A>G) | ClinVar dbSNP |
| 12 | g.25245355T>G | CA478892014 | KRAS | c.30A>C (p.Gly10=) c.-88+5396A>C (n.-88+5396A>C) | COSMIC COSMIC |
| 12 | g.25245355T= | CA2022898486 | KRAS | c.30A= (p.Gly10=) c.-88+5396A= (n.-88+5396A=) | |
| 12 | g.25245355_25245356insA | CA2580085332 | KRAS | c.29_30insT (p.Ala11SerfsTer23) c.-88+5395_-88+5396insT (n.-88+5395_-88+5396insT) | ClinVar |
| 12 | g.25245356C>A | CA384157477 | KRAS | c.29G>T (p.Gly10Val) c.-88+5395G>T (n.-88+5395G>T) | dbSNP COSMIC COSMIC |
| 12 | g.25245356C>G | CA384157475 | KRAS | c.29G>C (p.Gly10Ala) c.-88+5395G>C (n.-88+5395G>C) | dbSNP |
| 12 | g.25245356C>T | CA384157473 | KRAS | c.29G>A (p.Gly10Glu) c.-88+5395G>A (n.-88+5395G>A) | COSMIC COSMIC |
| 12 | g.25245357del | CA645572143 | KRAS | c.29del (p.Gly10GlufsTer5) c.-88+5395del (n.-88+5395del) | COSMIC |
| 12 | g.25245356_25245358dup | CA280165 | KRAS | c.27_29dup (p.Gly10_Ala11insGly) c.-88+5393_-88+5395dup (n.-88+5393_-88+5395dup) | ClinVar dbSNP |
| 12 | g.25245357C>A | CA384157479 | KRAS | c.28G>T (p.Gly10Ter) c.-88+5394G>T (n.-88+5394G>T) | dbSNP |
| 12 | g.25245357C>G | CA384157480 | KRAS | c.28G>C (p.Gly10Arg) c.-88+5394G>C (n.-88+5394G>C) | dbSNP |
| 12 | g.25245357C>T | CA384157482 | KRAS | c.28G>A (p.Gly10Arg) c.-88+5394G>A (n.-88+5394G>A) | dbSNP COSMIC COSMIC |
| 12 | g.25245357_25245358insTAC | CA645572144 | KRAS | c.28_29insTAG (p.Val9_Gly10insVal) c.-88+5394_-88+5395insTAG (n.-88+5394_-88+5395insTAG) | COSMIC |
| 12 | g.25245357_25245358insGAG | CA2580085333 | KRAS | c.27_28insCTC (p.Val9_Gly10insLeu) c.-88+5393_-88+5394insCTC (n.-88+5393_-88+5394insCTC) | ClinVar |
| 12 | g.25245358A>C | CA478892025 | KRAS | c.27T>G (p.Val9=) c.-88+5393T>G (n.-88+5393T>G) | ClinVar |
| 12 | g.25245358A>G | CA478892027 | KRAS | c.27T>C (p.Val9=) c.-88+5393T>C (n.-88+5393T>C) | COSMIC |
| 12 | g.25245358A>T | CA478892029 | KRAS | c.27T>A (p.Val9=) c.-88+5393T>A (n.-88+5393T>A) | ClinVar |
| 12 | g.25245359A>C | CA384157484 | KRAS | c.26T>G (p.Val9Gly) c.-88+5392T>G (n.-88+5392T>G) | dbSNP |
| 12 | g.25245359A>G | CA384157486 | KRAS | c.26T>C (p.Val9Ala) c.-88+5392T>C (n.-88+5392T>C) | dbSNP |
| 12 | g.25245359A>T | CA384157487 | KRAS | c.26T>A (p.Val9Asp) c.-88+5392T>A (n.-88+5392T>A) | COSMIC COSMIC |
| 12 | g.25245360C>A | CA384157491 | KRAS | c.25G>T (p.Val9Phe) c.-88+5391G>T (n.-88+5391G>T) | |
| 12 | g.25245360C= | CA2022898501 | KRAS | c.25G= (p.Val9=) c.-88+5391G= (n.-88+5391G=) | |
| 12 | g.25245360C>G | CA384157493 | KRAS | c.25G>C (p.Val9Leu) c.-88+5391G>C (n.-88+5391G>C) | dbSNP |
| 12 | g.25245360C>T | CA384157489 | KRAS | c.25G>A (p.Val9Ile) c.-88+5391G>A (n.-88+5391G>A) | dbSNP COSMIC COSMIC |
| 12 | g.25245361T>A | CA478892041 | KRAS | c.24A>T (p.Val8=) c.-88+5390A>T (n.-88+5390A>T) | dbSNP |
| 12 | g.25245361T>C | CA135558 | KRAS | c.24A>G (p.Val8=) c.-88+5390A>G (n.-88+5390A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.25245361T>G | CA478892043 | KRAS | c.24A>C (p.Val8=) c.-88+5390A>C (n.-88+5390A>C) | |
| 12 | g.25245361T= | CA2022898521 | KRAS | c.24A= (p.Val8=) c.-88+5390A= (n.-88+5390A=) | |
| 12 | g.25245361dup | CA2580085334 | KRAS | c.24dup (p.Val9SerfsTer25) c.-88+5390dup (n.-88+5390dup) | ClinVar |
| 12 | g.25245362A>C | CA384157495 | KRAS | c.23T>G (p.Val8Gly) c.-88+5389T>G (n.-88+5389T>G) | |
| 12 | g.25245362A>G | CA384157498 | KRAS | c.23T>C (p.Val8Ala) c.-88+5389T>C (n.-88+5389T>C) | |
| 12 | g.25245362A>T | CA384157496 | KRAS | c.23T>A (p.Val8Glu) c.-88+5389T>A (n.-88+5389T>A) | |
| 12 | g.25245363C>A | CA384157500 | KRAS | c.22G>T (p.Val8Leu) c.-88+5388G>T (n.-88+5388G>T) | dbSNP |
| 12 | g.25245363C>G | CA384157502 | KRAS | c.22G>C (p.Val8Leu) c.-88+5388G>C (n.-88+5388G>C) | dbSNP |