Linked Data
COSMIC:
COSM1283187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736159C>A , CM000685.2:g.153736159C>A | GRCh38 |
| NC_000023.10:g.153001613C>A , CM000685.1:g.153001613C>A | GRCh37 |
| NC_000023.9:g.152654807C>A | NCBI36 |
| NG_009022.2:g.16292C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1129C>A MANE Select | ENSP00000218104.3:p.Leu377Met | |
| ENST00000218104.5:c.1129C>A | ENSP00000218104.3:p.Leu377Met | |
| ENST00000443684.2:n.132C>A | ||
| NM_000033.3:c.1129C>A | NP_000024.2:p.Leu377Met | |
| XR_938507.1:n.1545C>A | ||
| XR_938507.2:n.1545C>A | ||
| NM_000033.4:c.1129C>A MANE Select | NP_000024.2:p.Leu377Met |