HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95324243_95324244delinsAC , CM000669.2:g.95324243_95324244delinsAC | GRCh38 |
NC_000007.13:g.94953555_94953556delinsAC , CM000669.1:g.94953555_94953556delinsAC | GRCh37 |
NC_000007.12:g.94791491_94791492delinsAC | NCBI36 |
NG_008779.1:g.5329_5330delinsGT | |
NG_008779.2:g.5463_5464delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.74+158_74+159delinsGT MANE Select | ENSP00000222381.3:n.74+158_74+159delinsGT | |
ENST00000222381.7:c.74+158_74+159delinsGT | ENSP00000222381.3:n.74+158_74+159delinsGT | |
ENST00000433729.1:c.74+158_74+159delinsGT | ENSP00000407359.1:n.74+158_74+159delinsGT | |
NM_000446.5:c.74+158_74+159delinsGT | NP_000437.3:n.74+158_74+159delinsGT | |
NM_000446.6:c.74+158_74+159delinsGT | NP_000437.3:n.74+158_74+159delinsGT | |
NM_000446.7:c.74+158_74+159delinsGT MANE Select | NP_000437.3:n.74+158_74+159delinsGT |