HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94781858_94781859delinsCG , CM000672.2:g.94781858_94781859delinsCG | GRCh38 |
NC_000010.10:g.96541615_96541616delinsCG , CM000672.1:g.96541615_96541616delinsCG | GRCh37 |
NC_000010.9:g.96531605_96531606delinsCG | NCBI36 |
NG_008384.2:g.24153_24154delinsCG | |
NG_008384.3:g.24178_24179delinsCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.680_681delinsCG MANE Select | ENSP00000360372.3:p.Pro227= | |
ENST00000645461.1:n.1733_1734delinsCG | ||
ENST00000371321.7:c.680_681delinsCG | ENSP00000360372.3:p.Pro227= | |
ENST00000464755.1:c.1443_1444delinsCG | ENSP00000483243.1:n.1443_1444delinsCG | |
NM_000769.2:c.680_681delinsCG | NP_000760.1:p.Pro227= | |
NM_000769.4:c.680_681delinsCG MANE Select | NP_000760.1:p.Pro227= |