Linked Data
ClinVar Variation Id:
1122767
ClinVar RCV Id:
RCV001453562
dbSNP Id:
rs2133982379
MyVariant Identifiers:
chr11:g.532717G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.532717G>T , CM000673.2:g.532717G>T | GRCh38 |
| NC_000011.9:g.532717G>T , CM000673.1:g.532717G>T | GRCh37 |
| NC_000011.8:g.522717G>T | NCBI36 |
| NG_007666.1:g.7834C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.*20-87C>A (HRAS) | ENSP00000380722.3:n.*20-87C>A | |
| ENST00000417302.7:c.*58C>A (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.*58C>A | |
| ENST00000397594.6:c.251-87C>A (HRAS) | ENSP00000380722.2:n.251-87C>A | |
| ENST00000417302.6:c.*58C>A (HRAS) | ENSP00000388246.1:n.*58C>A | |
| ENST00000462734.2:c.*101C>A (HRAS) | ENSP00000507303.1:n.*101C>A | |
| ENST00000311189.8:c.489C>A (HRAS) MANE Select | ENSP00000309845.7:p.Ile163= | |
| ENST00000311189.7:c.489C>A (HRAS) | ENSP00000309845.7:p.Ile163= | |
| ENST00000397594.5:c.*58C>A (HRAS) | ENSP00000380722.1:n.*58C>A | |
| ENST00000397596.6:c.489C>A (HRAS) | ENSP00000380723.2:p.Ile163= | |
| ENST00000417302.5:c.*58C>A (HRAS) | ENSP00000388246.1:n.*58C>A | |
| ENST00000451590.5:c.489C>A (HRAS) | ENSP00000407586.1:p.Ile163= | |
| ENST00000462734.1:n.264C>A (HRAS) | ||
| ENST00000478324.5:n.243-87C>A (HRAS) | ||
| ENST00000479482.1:n.410C>A (HRAS) | ||
| ENST00000493230.5:c.*58C>A (HRAS) | ENSP00000434023.1:n.*58C>A | |
| NM_001130442.1:c.489C>A (HRAS) | NP_001123914.1:p.Ile163= | |
| NM_005343.2:c.489C>A (HRAS) | NP_005334.1:p.Ile163= | |
| NM_176795.3:c.*58C>A (HRAS) | NP_789765.1:n.*58C>A | |
| XM_011519875.1:c.-425+4380G>T (LRRC56) | XP_011518177.1:n.-425+4380G>T | |
| XM_011519877.1:c.-162+4380G>T (LRRC56) | XP_011518179.1:n.-162+4380G>T | |
| XR_242795.1:n.770C>A (HRAS) | ||
| NM_001130442.2:c.489C>A (HRAS) | NP_001123914.1:p.Ile163= | |
| NM_001318054.1:c.252C>A (HRAS) | NP_001304983.1:p.Ile84= | |
| NM_005343.3:c.489C>A (HRAS) | NP_005334.1:p.Ile163= | |
| NM_176795.4:c.*58C>A (HRAS) | NP_789765.1:n.*58C>A | |
| XM_011519875.2:c.-425+4380G>T (LRRC56) | XP_011518177.1:n.-425+4380G>T | |
| XM_011519877.2:c.-162+4380G>T (LRRC56) | XP_011518179.1:n.-162+4380G>T | |
| XM_017017167.1:c.-500+4380G>T (LRRC56) | XP_016872656.1:n.-500+4380G>T | |
| XM_017017168.1:c.-500+4380G>T (LRRC56) | XP_016872657.1:n.-500+4380G>T | |
| NM_005343.4:c.489C>A (HRAS) MANE Select | NP_005334.1:p.Ile163= | |
| NM_001318054.2:c.252C>A (HRAS) | NP_001304983.1:p.Ile84= | |
| NM_001130442.3:c.489C>A (HRAS) | NP_001123914.1:p.Ile163= | |
| NM_176795.5:c.*58C>A (HRAS) MANE Plus Clinical | NP_789765.1:n.*58C>A |