Linked Data
COSMIC:
COSM4566270
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152311495_152311496delinsAA , CM000663.2:g.152311495_152311496delinsAA | GRCh38 |
| NC_000001.10:g.152283971_152283972delinsAA , CM000663.1:g.152283971_152283972delinsAA | GRCh37 |
| NC_000001.9:g.150550595_150550596delinsAA | NCBI36 |
| NG_016190.1:g.18708_18709delinsTT , LRG_1028:g.18708_18709delinsTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.3390_3391delinsTT MANE Select | ENSP00000357789.1:p.His1131Tyr | |
| ENST00000368799.1:c.3390_3391delinsTT | ENSP00000357789.1:p.His1131Tyr | |
| NM_002016.1:c.3390_3391delinsTT , LRG_1028t1:c.3390_3391delinsTT | NP_002007.1:p.His1131Tyr | |
| XM_011509329.1:c.3390_3391delinsTT | XP_011507631.1:p.His1131Tyr | |
| NM_002016.2:c.3390_3391delinsTT MANE Select | NP_002007.1:p.His1131Tyr |