Linked Data
COSMIC:
COSM4516765
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24799748_24799749delinsTT , CM000666.2:g.24799748_24799749delinsTT | GRCh38 |
| NC_000004.11:g.24801370_24801371delinsTT , CM000666.1:g.24801370_24801371delinsTT | GRCh37 |
| NC_000004.10:g.24410468_24410469delinsTT | NCBI36 |
| NG_012213.1:g.9286_9287delinsTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.227_228delinsTT MANE Select | ENSP00000371554.3:p.Pro76Leu | |
| ENST00000382120.3:c.227_228delinsTT | ENSP00000371554.3:p.Pro76Leu | |
| NM_003102.2:c.227_228delinsTT | NP_003093.2:p.Pro76Leu | |
| XR_427488.1:n.417_418delinsTT | ||
| NM_003102.3:c.227_228delinsTT | NP_003093.2:p.Pro76Leu | |
| NM_003102.4:c.227_228delinsTT MANE Select | NP_003093.2:p.Pro76Leu |