Linked Data
ClinVar Variation Id:
376292
ClinVar RCV Id:
RCV000420521
dbSNP Id:
rs121913336
COSMIC:
COSM465
PubMed:
PMID:25157968
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140753374G>C , CM000669.2:g.140753374G>C | GRCh38 |
| NC_000007.13:g.140453174G>C , CM000669.1:g.140453174G>C | GRCh37 |
| NC_000007.12:g.140099643G>C | NCBI36 |
| NG_007873.3:g.176391C>G , LRG_299:g.176391C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1761C>G MANE Select | ENSP00000493543.1:p.Asp587Glu | |
| ENST00000288602.11:c.1881C>G | ENSP00000288602.7:p.Asp627Glu | |
| ENST00000479537.6:c.431C>G | ||
| ENST00000496384.7:c.1761C>G | ENSP00000419060.2:p.Asp587Glu | |
| ENST00000497784.2:c.*1211C>G | ENSP00000420119.2:n.*1211C>G | |
| ENST00000642228.1:c.*839C>G | ENSP00000493678.1:n.*839C>G | |
| ENST00000642875.1:n.1259-3956C>G | ||
| ENST00000644120.1:n.2151C>G | ||
| ENST00000644650.1:c.857C>G | ||
| ENST00000644905.1:n.2643C>G | ||
| ENST00000644969.2:c.1881C>G MANE Plus Clinical | ENSP00000496776.1:p.Asp627Glu | |
| ENST00000646730.1:c.*337C>G | ENSP00000494784.1:n.*337C>G | |
| ENST00000646891.1:c.1761C>G | ENSP00000493543.1:p.Asp587Glu | |
| ENST00000647434.1:c.738-3956C>G | ENSP00000495132.1:n.738-3956C>G | |
| ENST00000288602.10:c.1761C>G | ENSP00000288602.6:p.Asp587Glu | |
| ENST00000479537.5:c.45C>G | ENSP00000418033.1:p.Asp15Glu | |
| ENST00000496384.6:c.584C>G | ||
| ENST00000497784.1:c.1796C>G | ENSP00000420119.1:n.1796C>G | |
| NM_004333.4:c.1761C>G , LRG_299t1:c.1761C>G | NP_004324.2:p.Asp587Glu | |
| XM_005250045.1:c.1761C>G | XP_005250102.1:p.Asp587Glu | |
| XM_005250046.1:c.1761C>G | XP_005250103.1:p.Asp587Glu | |
| XM_011516529.1:c.1761C>G | XP_011514831.1:p.Asp587Glu | |
| XM_011516530.1:c.1695-3956C>G | XP_011514832.1:n.1695-3956C>G | |
| XR_242190.1:n.1769C>G | ||
| XR_927520.1:n.1769C>G | ||
| XR_927521.1:n.1769C>G | ||
| XR_927522.1:n.1703-3956C>G | ||
| XR_927523.1:n.1703-3956C>G | ||
| NM_001354609.1:c.1761C>G | NP_001341538.1:p.Asp587Glu | |
| NM_004333.5:c.1761C>G | NP_004324.2:p.Asp587Glu | |
| NR_148928.1:n.2859C>G | ||
| XM_017012558.1:c.1881C>G | XP_016868047.1:p.Asp627Glu | |
| XM_017012559.1:c.1881C>G | XP_016868048.1:p.Asp627Glu | |
| XR_001744857.1:n.1889C>G | ||
| XR_001744858.1:n.1823-3956C>G | ||
| NM_001354609.2:c.1761C>G | NP_001341538.1:p.Asp587Glu | |
| NM_001374244.1:c.1881C>G | NP_001361173.1:p.Asp627Glu | |
| NM_001374258.1:c.1881C>G MANE Plus Clinical | NP_001361187.1:p.Asp627Glu | |
| NM_004333.6:c.1761C>G MANE Select | NP_004324.2:p.Asp587Glu | |
| NM_001378467.1:c.1770C>G | NP_001365396.1:p.Asp590Glu | |
| NM_001378468.1:c.1761C>G | NP_001365397.1:p.Asp587Glu | |
| NM_001378469.1:c.1695C>G | NP_001365398.1:p.Asp565Glu | |
| NM_001378470.1:c.1659C>G | NP_001365399.1:p.Asp553Glu | |
| NM_001378471.1:c.1650C>G | NP_001365400.1:p.Asp550Glu | |
| NM_001378472.1:c.1605C>G | NP_001365401.1:p.Asp535Glu | |
| NM_001378473.1:c.1605C>G | NP_001365402.1:p.Asp535Glu | |
| NM_001378474.1:c.1761C>G | NP_001365403.1:p.Asp587Glu | |
| NM_001378475.1:c.1497C>G | NP_001365404.1:p.Asp499Glu |