HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269090del , CM000668.2:g.31269090del | GRCh38 |
NC_000006.11:g.31236867del , CM000668.1:g.31236867del | GRCh37 |
NC_000006.10:g.31344846del | NCBI36 |
NG_029422.2:g.8044del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*81del MANE Select | ENSP00000365402.5:n.*81del | |
ENST00000376228.9:c.*81del | ENSP00000365402.5:n.*81del | |
ENST00000376237.8:c.*769del | ENSP00000365412.4:n.*769del | |
ENST00000383329.7:c.*81del | ENSP00000372819.3:n.*81del | |
ENST00000466892.5:n.415del | ||
ENST00000470363.5:n.940del | ||
ENST00000487245.5:n.1541del | ||
NM_002117.5:c.*81del | NP_002108.4:n.*81del | |
NM_002117.6:c.*81del MANE Select | NP_002108.4:n.*81del |