HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15930677_15930681delinsTAAAG , CM000663.2:g.15930677_15930681delinsTAAAG | GRCh38 |
NC_000001.10:g.16257172_16257176delinsTAAAG , CM000663.1:g.16257172_16257176delinsTAAAG | GRCh37 |
NC_000001.9:g.16129759_16129763delinsTAAAG | NCBI36 |
NG_050663.1:g.87814_87818delinsTAAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000438066.2:c.*5288_*5292delinsTAAAG | ENSP00000388021.2:n.*5288_*5292delinsTAAA... | |
ENST00000704274.1:c.34_38delinsTAAAG | ||
ENST00000375759.8:c.4437_4441delinsTAAAG MANE Select | ENSP00000364912.3:p.Asp1479= | |
ENST00000375759.7:c.4437_4441delinsTAAAG | ENSP00000364912.3:p.Asp1479= | |
NM_015001.2:c.4437_4441delinsTAAAG | NP_055816.2:p.Asp1479= | |
NM_015001.3:c.4437_4441delinsTAAAG MANE Select | NP_055816.2:p.Asp1479= |