Linked Data
COSMIC:
COSM3981538
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48411001A>T , CM000677.2:g.48411001A>T | GRCh38 |
| NC_000015.9:g.48703198A>T , CM000677.1:g.48703198A>T | GRCh37 |
| NC_000015.8:g.46490490A>T | NCBI36 |
| NG_008805.2:g.239788T>A , LRG_778:g.239788T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1413T>A | ENSP00000453958.2:n.*1413T>A | |
| ENST00000682158.1:n.1986T>A | ||
| ENST00000682170.1:n.2786T>A | ||
| ENST00000682767.1:n.1902T>A | ||
| ENST00000316623.10:c.8605T>A MANE Select | ENSP00000325527.5:p.Leu2869Met | |
| ENST00000316623.9:c.8605T>A | ENSP00000325527.5:p.Leu2869Met | |
| ENST00000559133.5:c.3974T>A | ||
| NM_000138.4:c.8605T>A , LRG_778t1:c.8605T>A | NP_000129.3:p.Leu2869Met | |
| NM_000138.5:c.8605T>A MANE Select | NP_000129.3:p.Leu2869Met |