Linked Data
COSMIC:
COSM6184732
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033601G>T , CM000685.2:g.106033601G>T | GRCh38 |
| NC_000023.10:g.105277592G>T , CM000685.1:g.105277592G>T | GRCh37 |
| NC_000023.9:g.105164248G>T | NCBI36 |
| NG_021252.1:g.10127C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.1147C>A MANE Select | ENSP00000361644.1:p.Pro383Thr | |
| ENST00000327674.8:c.1147C>A | ENSP00000329374.4:p.Pro383Thr | |
| ENST00000372563.1:c.1147C>A | ENSP00000361644.1:p.Pro383Thr | |
| NM_000354.5:c.1147C>A | NP_000345.2:p.Pro383Thr | |
| XM_006724683.1:c.1177C>A | XP_006724746.1:p.Pro393Thr | |
| XM_005262180.4:c.*92C>A | XP_005262237.1:n.*92C>A | |
| XM_006724683.2:c.1177C>A | XP_006724746.1:p.Pro393Thr | |
| NM_000354.6:c.1147C>A MANE Select | NP_000345.2:p.Pro383Thr |