Canonical Allele Identifier: CA1788099467
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60852117C= , CM000670.2:g.60852117C= GRCh38
NC_000008.10:g.61764676C= , CM000670.1:g.61764676C= GRCh37
NC_000008.9:g.61927230C= NCBI36
NG_007009.1:g.178338C= , LRG_176:g.178338C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695853.1:c.5764C= ENSP00000512218.1:p.Arg1922=
ENST00000423902.7:c.5764C= MANE Select ENSP00000392028.1:p.Arg1922=
ENST00000423902.6:c.5764C= ENSP00000392028.1:p.Arg1922=
ENST00000524602.5:c.1717-10112C= ENSP00000437061.1:n.1717-10112C=
ENST00000527921.1:n.255C=
NM_001316690.1:c.1717-10112C= NP_001303619.1:n.1717-10112C=
NM_017780.3:c.5764C= NP_060250.2:p.Arg1922=
XM_011517553.1:c.5854C= XP_011515855.1:p.Arg1952=
XM_011517554.1:c.5854C= XP_011515856.1:p.Arg1952=
XM_011517555.1:c.5854C= XP_011515857.1:p.Arg1952=
XM_011517556.1:c.5854C= XP_011515858.1:p.Arg1952=
XM_011517557.1:c.3841C= XP_011515859.1:p.Arg1281=
XM_011517558.1:c.3391C= XP_011515860.1:p.Arg1131=
XM_011517559.1:c.2599C= XP_011515861.1:p.Arg867=
XM_011517553.2:c.5854C= XP_011515855.1:p.Arg1952=
XM_011517554.3:c.5854C= XP_011515856.1:p.Arg1952=
XM_011517555.2:c.5854C= XP_011515857.1:p.Arg1952=
XM_017013612.1:c.5854C= XP_016869101.1:p.Arg1952=
XM_017013613.1:c.5764C= XP_016869102.1:p.Arg1922=
NM_017780.4:c.5764C= MANE Select NP_060250.2:p.Arg1922=