Canonical Allele Identifier: CA1788120837

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861021G= , CM000670.2:g.60861021G=	GRCh38
NC_000008.10:g.61773580G= , CM000670.1:g.61773580G=	GRCh37
NC_000008.9:g.61936134G=	NCBI36
NG_007009.1:g.187242G= , LRG_176:g.187242G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.902G=
ENST00000695851.1:n.106G=
ENST00000695853.1:c.*785G=	ENSP00000512218.1:n.*785G=
ENST00000423902.7:c.7726G= MANE Select	ENSP00000392028.1:p.Asp2576=
ENST00000423902.6:c.7726G=	ENSP00000392028.1:p.Asp2576=
ENST00000524602.5:c.1717-1208G=	ENSP00000437061.1:n.1717-1208G=
ENST00000531695.1:n.150G=
ENST00000618450.1:n.118G=
NM_001316690.1:c.1717-1208G=	NP_001303619.1:n.1717-1208G=
NM_017780.3:c.7726G=	NP_060250.2:p.Asp2576=
XM_011517553.1:c.7816G=	XP_011515855.1:p.Asp2606=
XM_011517554.1:c.7816G=	XP_011515856.1:p.Asp2606=
XM_011517555.1:c.7813G=	XP_011515857.1:p.Asp2605=
XM_011517556.1:c.7699-1175G=	XP_011515858.1:n.7699-1175G=
XM_011517557.1:c.5803G=	XP_011515859.1:p.Asp1935=
XM_011517558.1:c.5353G=	XP_011515860.1:p.Asp1785=
XM_011517559.1:c.4561G=	XP_011515861.1:p.Asp1521=
XM_011517553.2:c.7816G=	XP_011515855.1:p.Asp2606=
XM_011517554.3:c.7816G=	XP_011515856.1:p.Asp2606=
XM_011517555.2:c.7813G=	XP_011515857.1:p.Asp2605=
XM_017013612.1:c.7816G=	XP_016869101.1:p.Asp2606=
XM_017013613.1:c.7723G=	XP_016869102.1:p.Asp2575=
NM_017780.4:c.7726G= MANE Select	NP_060250.2:p.Asp2576=