HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8015826del , CM000679.2:g.8015826del | GRCh38 |
NC_000017.10:g.7919144del , CM000679.1:g.7919144del | GRCh37 |
NC_000017.9:g.7859869del | NCBI36 |
NG_009092.1:g.18157del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.3028del MANE Select | ENSP00000254854.4:p.Glu1010SerfsTer11 | |
ENST00000254854.4:c.3028del | ENSP00000254854.4:p.Glu1010SerfsTer11 | |
NM_000180.3:c.3028del | NP_000171.1:p.Glu1010SerfsTer11 | |
XM_011523816.1:c.3028del | XP_011522118.1:p.Glu1010SerfsTer11 | |
NM_000180.4:c.3028del MANE Select | NP_000171.1:p.Glu1010SerfsTer11 |