Linked Data
ClinVar Variation Id:
376256
ClinVar RCV Id:
RCV000440432
dbSNP Id:
rs121913524
COSMIC:
COSM1323
PubMed:
PMID:25157968
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54733182T>C , CM000666.2:g.54733182T>C | GRCh38 |
| NC_000004.11:g.55599348T>C , CM000666.1:g.55599348T>C | GRCh37 |
| NC_000004.10:g.55294105T>C | NCBI36 |
| NG_007456.1:g.80188T>C , LRG_307:g.80188T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.2462T>C | ENSP00000390987.3:p.Val821Ala | |
| ENST00000685269.1:n.2552T>C | ||
| ENST00000686011.1:c.2459T>C | ENSP00000509704.1:p.Val820Ala | |
| ENST00000687109.1:c.2477T>C | ENSP00000509371.1:p.Val826Ala | |
| ENST00000687208.1:n.2886T>C | ||
| ENST00000687246.1:c.2349+1184T>C | ENSP00000509114.1:n.2349+1184T>C | |
| ENST00000687265.1:n.2632T>C | ||
| ENST00000687295.1:c.2462T>C | ENSP00000509450.1:p.Val821Ala | |
| ENST00000688060.1:n.271T>C | ||
| ENST00000688704.1:n.1486T>C | ||
| ENST00000689832.1:c.2474T>C | ENSP00000509084.1:p.Val825Ala | |
| ENST00000689994.1:c.1964T>C | ENSP00000509156.1:p.Val655Ala | |
| ENST00000690543.1:c.2465T>C | ENSP00000508831.1:p.Val822Ala | |
| ENST00000690917.1:n.2692T>C | ||
| ENST00000691361.1:n.1384T>C | ||
| ENST00000692783.1:c.2471T>C | ENSP00000508733.1:p.Val824Ala | |
| ENST00000692991.1:n.2571T>C | ||
| ENST00000288135.6:c.2474T>C MANE Select | ENSP00000288135.6:p.Val825Ala | |
| ENST00000288135.5:c.2474T>C | ENSP00000288135.5:p.Val825Ala | |
| ENST00000412167.6:c.2462T>C | ENSP00000390987.2:p.Val821Ala | |
| ENST00000512959.1:n.527T>C | ||
| NM_000222.2:c.2474T>C , LRG_307t1:c.2474T>C | NP_000213.1:p.Val825Ala | |
| NM_001093772.1:c.2462T>C | NP_001087241.1:p.Val821Ala | |
| XM_005265740.1:c.2477T>C | XP_005265797.1:p.Val826Ala | |
| XM_005265741.1:c.2474T>C | XP_005265798.1:p.Val825Ala | |
| XM_005265742.1:c.2465T>C | XP_005265799.1:p.Val822Ala | |
| XM_005265742.3:c.2465T>C | XP_005265799.1:p.Val822Ala | |
| XM_017008178.1:c.2471T>C | XP_016863667.1:p.Val824Ala | |
| XM_017008179.1:c.2462T>C | XP_016863668.1:p.Val821Ala | |
| XM_017008180.1:c.2459T>C | XP_016863669.1:p.Val820Ala | |
| NM_000222.3:c.2474T>C MANE Select | NP_000213.1:p.Val825Ala | |
| NM_001093772.2:c.2462T>C | NP_001087241.1:p.Val821Ala | |
| NM_001385284.1:c.2477T>C | NP_001372213.1:p.Val826Ala | |
| NM_001385285.1:c.2471T>C | NP_001372214.1:p.Val824Ala | |
| NM_001385286.1:c.2459T>C | NP_001372215.1:p.Val820Ala | |
| NM_001385288.1:c.2465T>C | NP_001372217.1:p.Val822Ala | |
| NM_001385290.1:c.2474T>C | NP_001372219.1:p.Val825Ala | |
| NM_001385292.1:c.2462T>C | NP_001372221.1:p.Val821Ala |