HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125004_55125005delinsTC , CM000666.2:g.55125004_55125005delinsTC | GRCh38 |
NC_000004.11:g.55991171_55991172delinsTC , CM000666.1:g.55991171_55991172delinsTC | GRCh37 |
NC_000004.10:g.55685928_55685929delinsTC | NCBI36 |
NG_012004.1:g.5591_5592delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.67+222_67+223delinsGA MANE Select | ENSP00000263923.4:n.67+222_67+223delinsGA | |
ENST00000263923.4:c.67+222_67+223delinsGA | ENSP00000263923.4:n.67+222_67+223delinsGA | |
ENST00000512566.1:n.67+222_67+223delinsGA | ||
NM_002253.2:c.67+222_67+223delinsGA | NP_002244.1:n.67+222_67+223delinsGA | |
NM_002253.3:c.67+222_67+223delinsGA | NP_002244.1:n.67+222_67+223delinsGA | |
NM_002253.4:c.67+222_67+223delinsGA MANE Select | NP_002244.1:n.67+222_67+223delinsGA |