HGVS | Genome Assembly |
---|---|
NC_000023.11:g.141895142del , CM000685.2:g.141895142del | GRCh38 |
NC_000023.10:g.140982928del , CM000685.1:g.140982928del | GRCh37 |
NC_000023.9:g.140810594del | NCBI36 |
NG_013272.1:g.61827del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000298296.1:c.910-127del MANE Select | ENSP00000298296.1:n.910-127del | |
ENST00000443323.2:c.-118-1289del | ENSP00000438254.1:n.-118-1289del | |
ENST00000483584.5:n.150-127del | ||
ENST00000544766.5:c.-378-127del | ENSP00000440444.1:n.-378-127del | |
NM_138702.1:c.910-127del MANE Select | NP_619647.1:n.910-127del | |
NM_177456.2:c.-378-127del | NP_803251.1:n.-378-127del | |
XM_017029265.2:c.-378-127del | XP_016884754.1:n.-378-127del |