Linked Data
COSMIC:
COSM3980292
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920074C>A , CM000679.2:g.74920074C>A | GRCh38 |
| NC_000017.10:g.72916169C>A , CM000679.1:g.72916169C>A | GRCh37 |
| NC_000017.9:g.70427764C>A | NCBI36 |
| NG_007882.1:g.8183G>T | |
| NG_033062.1:g.800C>A | |
| NG_007882.2:g.8190G>T | |
| NG_033062.2:g.800C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.762G>T MANE Select | ENSP00000480279.1:p.Met254Ile | |
| ENST00000579243.1:c.*361G>T | ENSP00000462568.1:n.*361G>T | |
| ENST00000614341.4:c.762G>T | ENSP00000480279.1:p.Met254Ile | |
| NM_001282489.2:c.453G>T | NP_001269418.1:p.Met151Ile | |
| NM_173477.4:c.762G>T | NP_775748.2:p.Met254Ile | |
| XM_011524296.1:c.453G>T | XP_011522598.1:p.Met151Ile | |
| XM_011524296.2:c.453G>T | XP_011522598.1:p.Met151Ile | |
| NM_173477.5:c.762G>T MANE Select | NP_775748.2:p.Met254Ile | |
| NM_001282489.3:c.453G>T | NP_001269418.1:p.Met151Ile |