Linked Data
COSMIC:
COSM351120
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135952878C>G , CM000667.2:g.135952878C>G | GRCh38 |
| NC_000005.9:g.135288567C>G , CM000667.1:g.135288567C>G | GRCh37 |
| NC_000005.8:g.135316466C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274507.6:c.136G>C MANE Select | ENSP00000274507.1:p.Ala46Pro | |
| ENST00000274507.5:c.136G>C | ENSP00000274507.1:p.Ala46Pro | |
| ENST00000471827.1:n.239G>C | ||
| ENST00000512872.1:c.-81G>C | ENSP00000427012.1:n.-81G>C | |
| ENST00000514447.2:c.136G>C | ENSP00000421123.2:p.Ala46Pro | |
| ENST00000522943.5:c.136G>C | ENSP00000429618.1:p.Ala46Pro | |
| NM_002302.2:c.136G>C | NP_002293.2:p.Ala46Pro | |
| NM_002302.3:c.136G>C MANE Select | NP_002293.2:p.Ala46Pro |