HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1013873del , CM000663.2:g.1013873del | GRCh38 |
NC_000001.10:g.949253del , CM000663.1:g.949253del | GRCh37 |
NC_000001.9:g.939116del | NCBI36 |
NG_033033.1:g.5407del | |
NG_033033.2:g.17736del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.-21-111del | ENSP00000485643.1:n.-21-111del | |
ENST00000649529.1:c.4-111del MANE Select | ENSP00000496832.1:n.4-111del | |
ENST00000379389.4:c.4-111del | ENSP00000368699.4:n.4-111del | |
ENST00000624652.1:c.-21-111del | ENSP00000485313.1:n.-21-111del | |
ENST00000624697.3:c.-21-111del | ENSP00000485643.1:n.-21-111del | |
NM_005101.3:c.4-111del | NP_005092.1:n.4-111del | |
NM_005101.4:c.4-111del MANE Select | NP_005092.1:n.4-111del |