HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29477705del , CM000679.2:g.29477705del | GRCh38 |
NC_000017.10:g.27804723del , CM000679.1:g.27804723del | GRCh37 |
NC_000017.9:g.24828849del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.351del MANE Select | ENSP00000261716.3:p.Val118PhefsTer11 | |
ENST00000261716.7:c.351del | ENSP00000261716.3:p.Val118PhefsTer11 | |
ENST00000536202.1:c.351del | ENSP00000438819.1:p.Val118PhefsTer11 | |
NM_020791.2:c.351del | NP_065842.1:p.Val118PhefsTer11 | |
NM_025142.1:c.351del | NP_079418.1:p.Val118PhefsTer11 | |
XM_011525060.1:c.351del | XP_011523362.1:p.Val118PhefsTer11 | |
XM_011525060.2:c.351del | XP_011523362.1:p.Val118PhefsTer11 | |
NM_020791.4:c.351del MANE Select | NP_065842.1:p.Val118PhefsTer11 |