Linked Data
COSMIC:
COSM331128
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160130544_160130545delinsAA , CM000663.2:g.160130544_160130545delinsAA | GRCh38 |
| NC_000001.10:g.160100334_160100335delinsAA , CM000663.1:g.160100334_160100335delinsAA | GRCh37 |
| NC_000001.9:g.158366958_158366959delinsAA | NCBI36 |
| NG_008014.1:g.19787_19788delinsAA , LRG_6:g.19787_19788delinsAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1774_1775delinsAA MANE Select | ENSP00000354490.3:p.Pro592Asn | |
| ENST00000361216.7:c.1774_1775delinsAA | ENSP00000354490.3:p.Pro592Asn | |
| ENST00000392233.7:c.1774_1775delinsAA | ENSP00000376066.3:p.Pro592Asn | |
| ENST00000447527.1:c.906_907delinsAA | ||
| ENST00000472488.5:n.1877_1878delinsAA | ||
| NM_000702.3:c.1774_1775delinsAA | NP_000693.1:p.Pro592Asn | |
| NM_000702.4:c.1774_1775delinsAA MANE Select | NP_000693.1:p.Pro592Asn |