HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734041_4734042del , CM000679.2:g.4734041_4734042del | GRCh38 |
NC_000017.10:g.4637336_4637337del , CM000679.1:g.4637336_4637337del | GRCh37 |
NC_000017.9:g.4584085_4584086del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*464_*465del MANE Select | ENSP00000293778.7:n.*464_*465del | |
ENST00000293778.10:c.*464_*465del | ENSP00000293778.6:n.*464_*465del | |
ENST00000576153.5:n.1020_1021del | ||
NM_022059.3:c.*464_*465del | NP_071342.2:n.*464_*465del | |
NM_022059.4:c.*464_*465del | NP_071342.2:n.*464_*465del | |
NM_001386809.1:c.*464_*465del MANE Select | NP_001373738.1:n.*464_*465del |