HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610872_1610874del , CM000668.2:g.1610872_1610874del | GRCh38 |
NC_000006.11:g.1611107_1611109del , CM000668.1:g.1611107_1611109del | GRCh37 |
NC_000006.10:g.1556106_1556108del | NCBI36 |
NG_009368.1:g.5427_5429del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.427_429del MANE Select | ENSP00000493906.1:p.Asp143del | |
ENST00000380874.3:c.427_429del | ENSP00000370256.2:p.Asp143del | |
NM_001453.2:c.427_429del | NP_001444.2:p.Asp143del | |
NM_001453.3:c.427_429del MANE Select | NP_001444.2:p.Asp143del |