Linked Data
COSMIC:
COSM3727191
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912568T>C , CM000674.2:g.4912568T>C | GRCh38 |
| NC_000012.11:g.5021734T>C , CM000674.1:g.5021734T>C | GRCh37 |
| NC_000012.10:g.4891995T>C | NCBI36 |
| NG_011815.1:g.7662T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.1190T>C MANE Select | ENSP00000371985.3:p.Val397Ala | |
| ENST00000543874.3:n.105+2096T>C | ||
| ENST00000639306.1:c.1028T>C | ENSP00000492506.1:p.Val343Ala | |
| ENST00000639680.1:c.76+302T>C | ||
| ENST00000382545.3:c.1190T>C | ENSP00000371985.3:p.Val397Ala | |
| ENST00000541095.1:n.105+2096T>C | ||
| ENST00000543874.2:n.96+2096T>C | ||
| NM_000217.2:c.1190T>C | NP_000208.2:p.Val397Ala | |
| NM_000217.3:c.1190T>C MANE Select | NP_000208.2:p.Val397Ala |