HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21178455_21178458delinsTTAC , CM000674.2:g.21178455_21178458delinsTTAC | GRCh38 |
NC_000012.11:g.21331389_21331392delinsTTAC , CM000674.1:g.21331389_21331392delinsTTAC | GRCh37 |
NC_000012.10:g.21222656_21222659delinsTTAC | NCBI36 |
NG_011745.1:g.52262_52265delinsTTAC , LRG_1022:g.52262_52265delinsTTAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.482-121_482-118delinsTTAC MANE Select | ENSP00000256958.2:n.482-121_482-118delinsTTAC | |
ENST00000256958.2:c.482-121_482-118delinsTTAC | ENSP00000256958.2:n.482-121_482-118delinsTTAC | |
NM_006446.4:c.482-121_482-118delinsTTAC , LRG_1022t1:c.482-121_482-118delinsTTAC | NP_006437.3:n.482-121_482-118delinsTTAC | |
NM_006446.5:c.482-121_482-118delinsTTAC MANE Select | NP_006437.3:n.482-121_482-118delinsTTAC |