HGVS | Genome Assembly |
---|---|
NC_000007.14:g.1234065_1234066delinsGA , CM000669.2:g.1234065_1234066delinsGA | GRCh38 |
NC_000007.13:g.1273701_1273702delinsGA , CM000669.1:g.1273701_1273702delinsGA | GRCh37 |
NC_000007.12:g.1240227_1240228delinsGA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000316333.9:c.450+370_450+371delinsGA MANE Select | ENSP00000314480.8:n.450+370_450+371delins... | |
ENST00000316333.8:c.450+370_450+371delinsGA | ENSP00000314480.8:n.450+370_450+371delins... | |
NM_001080461.1:c.450+370_450+371delinsGA | NP_001073930.1:n.450+370_450+371delinsGA | |
NM_001080461.2:c.450+370_450+371delinsGA | NP_001073930.1:n.450+370_450+371delinsGA | |
NM_001080461.3:c.450+370_450+371delinsGA MANE Select | NP_001073930.1:n.450+370_450+371delinsGA |