Linked Data
COSMIC:
COSM317372
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152312305_152312306delinsTT , CM000663.2:g.152312305_152312306delinsTT | GRCh38 |
| NC_000001.10:g.152284781_152284782delinsTT , CM000663.1:g.152284781_152284782delinsTT | GRCh37 |
| NC_000001.9:g.150551405_150551406delinsTT | NCBI36 |
| NG_016190.1:g.17898_17899delinsAA , LRG_1028:g.17898_17899delinsAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.2580_2581delinsAA MANE Select | ENSP00000357789.1:p.Val861Ile | |
| ENST00000368799.1:c.2580_2581delinsAA | ENSP00000357789.1:p.Val861Ile | |
| NM_002016.1:c.2580_2581delinsAA , LRG_1028t1:c.2580_2581delinsAA | NP_002007.1:p.Val861Ile | |
| XM_011509329.1:c.2580_2581delinsAA | XP_011507631.1:p.Val861Ile | |
| NM_002016.2:c.2580_2581delinsAA MANE Select | NP_002007.1:p.Val861Ile |