HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133353896_133353897delinsCT , CM000671.2:g.133353896_133353897delinsCT | GRCh38 |
NC_000009.10:g.135210572_135210573delinsCT | NCBI36 |
NG_008477.1:g.7610_7611delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.367_368delinsAG MANE Select | ENSP00000361042.3:p.Arg123= | |
ENST00000371974.7:c.367_368delinsAG | ENSP00000361042.3:p.Arg123= | |
ENST00000437995.1:n.313_314delinsAG | ||
ENST00000495952.5:n.357_358delinsAG | ||
ENST00000615505.4:c.40_41delinsAG | ENSP00000482067.1:p.Arg14= | |
NM_001280787.1:c.40_41delinsAG | NP_001267716.1:p.Arg14= | |
NM_003172.3:c.367_368delinsAG | NP_003163.1:p.Arg123= | |
XM_011518942.1:c.40_41delinsAG | XP_011517244.1:p.Arg14= | |
NM_003172.4:c.367_368delinsAG MANE Select | NP_003163.1:p.Arg123= |