Linked Data
ClinVar Variation Id:
40388
dbSNP Id:
rs121913375
COSMIC:
COSM472
ERepo:
CA281995/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140753339G>A , CM000669.2:g.140753339G>A | GRCh38 |
| NC_000007.13:g.140453139G>A , CM000669.1:g.140453139G>A | GRCh37 |
| NC_000007.12:g.140099608G>A | NCBI36 |
| NG_007873.3:g.176426C>T , LRG_299:g.176426C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1796C>T MANE Select | ENSP00000493543.1:p.Thr599Ile | |
| ENST00000288602.11:c.1916C>T | ENSP00000288602.7:p.Thr639Ile | |
| ENST00000479537.6:c.466C>T | ||
| ENST00000496384.7:c.1796C>T | ENSP00000419060.2:p.Thr599Ile | |
| ENST00000497784.2:c.*1246C>T | ENSP00000420119.2:n.*1246C>T | |
| ENST00000642228.1:c.*874C>T | ENSP00000493678.1:n.*874C>T | |
| ENST00000642875.1:n.1259-3921C>T | ||
| ENST00000644120.1:n.2186C>T | ||
| ENST00000644650.1:c.892C>T | ||
| ENST00000644905.1:n.2678C>T | ||
| ENST00000644969.2:c.1916C>T MANE Plus Clinical | ENSP00000496776.1:p.Thr639Ile | |
| ENST00000646730.1:c.*372C>T | ENSP00000494784.1:n.*372C>T | |
| ENST00000646891.1:c.1796C>T | ENSP00000493543.1:p.Thr599Ile | |
| ENST00000647434.1:c.738-3921C>T | ENSP00000495132.1:n.738-3921C>T | |
| ENST00000288602.10:c.1796C>T | ENSP00000288602.6:p.Thr599Ile | |
| ENST00000479537.5:c.80C>T | ENSP00000418033.1:p.Thr27Ile | |
| ENST00000496384.6:c.619C>T | ||
| ENST00000497784.1:c.1831C>T | ENSP00000420119.1:n.1831C>T | |
| NM_004333.4:c.1796C>T , LRG_299t1:c.1796C>T | NP_004324.2:p.Thr599Ile | |
| XM_005250045.1:c.1796C>T | XP_005250102.1:p.Thr599Ile | |
| XM_005250046.1:c.1796C>T | XP_005250103.1:p.Thr599Ile | |
| XM_011516529.1:c.1796C>T | XP_011514831.1:p.Thr599Ile | |
| XM_011516530.1:c.1695-3921C>T | XP_011514832.1:n.1695-3921C>T | |
| XR_242190.1:n.1804C>T | ||
| XR_927520.1:n.1804C>T | ||
| XR_927521.1:n.1804C>T | ||
| XR_927522.1:n.1703-3921C>T | ||
| XR_927523.1:n.1703-3921C>T | ||
| NM_001354609.1:c.1796C>T | NP_001341538.1:p.Thr599Ile | |
| NM_004333.5:c.1796C>T | NP_004324.2:p.Thr599Ile | |
| NR_148928.1:n.2894C>T | ||
| XM_017012558.1:c.1916C>T | XP_016868047.1:p.Thr639Ile | |
| XM_017012559.1:c.1916C>T | XP_016868048.1:p.Thr639Ile | |
| XR_001744857.1:n.1924C>T | ||
| XR_001744858.1:n.1823-3921C>T | ||
| NM_001354609.2:c.1796C>T | NP_001341538.1:p.Thr599Ile | |
| NM_001374244.1:c.1916C>T | NP_001361173.1:p.Thr639Ile | |
| NM_001374258.1:c.1916C>T MANE Plus Clinical | NP_001361187.1:p.Thr639Ile | |
| NM_004333.6:c.1796C>T MANE Select | NP_004324.2:p.Thr599Ile | |
| NM_001378467.1:c.1805C>T | NP_001365396.1:p.Thr602Ile | |
| NM_001378468.1:c.1796C>T | NP_001365397.1:p.Thr599Ile | |
| NM_001378469.1:c.1730C>T | NP_001365398.1:p.Thr577Ile | |
| NM_001378470.1:c.1694C>T | NP_001365399.1:p.Thr565Ile | |
| NM_001378471.1:c.1685C>T | NP_001365400.1:p.Thr562Ile | |
| NM_001378472.1:c.1640C>T | NP_001365401.1:p.Thr547Ile | |
| NM_001378473.1:c.1640C>T | NP_001365402.1:p.Thr547Ile | |
| NM_001378474.1:c.1796C>T | NP_001365403.1:p.Thr599Ile | |
| NM_001378475.1:c.1532C>T | NP_001365404.1:p.Thr511Ile |