HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811751_55811752del , CM000673.2:g.55811751_55811752del | GRCh38 |
NC_000011.9:g.55579227_55579228del , CM000673.1:g.55579227_55579228del | GRCh37 |
NC_000011.8:g.55335803_55335804del | NCBI36 |
NG_052620.1:g.5385_5386del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.285_286del MANE Select | ENSP00000485319.1:p.Gly96ValfsTer15 | |
ENST00000333973.3:c.285_286del | ENSP00000335529.2:p.Gly96ValfsTer15 | |
ENST00000623450.1:c.285_286del | ENSP00000485509.1:p.Gly96ValfsTer15 | |
ENST00000625203.1:c.285_286del | ENSP00000485319.1:p.Gly96ValfsTer15 | |
NM_001004738.1:c.285_286del | NP_001004738.1:p.Gly96ValfsTer15 | |
NM_001004738.2:c.285_286del MANE Select | NP_001004738.1:p.Gly96ValfsTer15 |