Canonical Allele Identifier: CA1788120778

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860998G= , CM000670.2:g.60860998G=	GRCh38
NC_000008.10:g.61773557G= , CM000670.1:g.61773557G=	GRCh37
NC_000008.9:g.61936111G=	NCBI36
NG_007009.1:g.187219G= , LRG_176:g.187219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.879G=
ENST00000695851.1:n.83G=
ENST00000695853.1:c.*762G=	ENSP00000512218.1:n.*762G=
ENST00000423902.7:c.7703G= MANE Select	ENSP00000392028.1:p.Arg2568=
ENST00000423902.6:c.7703G=	ENSP00000392028.1:p.Arg2568=
ENST00000524602.5:c.1717-1231G=	ENSP00000437061.1:n.1717-1231G=
ENST00000531695.1:n.127G=
ENST00000618450.1:n.95G=
NM_001316690.1:c.1717-1231G=	NP_001303619.1:n.1717-1231G=
NM_017780.3:c.7703G=	NP_060250.2:p.Arg2568=
XM_011517553.1:c.7793G=	XP_011515855.1:p.Arg2598=
XM_011517554.1:c.7793G=	XP_011515856.1:p.Arg2598=
XM_011517555.1:c.7790G=	XP_011515857.1:p.Arg2597=
XM_011517556.1:c.7699-1198G=	XP_011515858.1:n.7699-1198G=
XM_011517557.1:c.5780G=	XP_011515859.1:p.Arg1927=
XM_011517558.1:c.5330G=	XP_011515860.1:p.Arg1777=
XM_011517559.1:c.4538G=	XP_011515861.1:p.Arg1513=
XM_011517553.2:c.7793G=	XP_011515855.1:p.Arg2598=
XM_011517554.3:c.7793G=	XP_011515856.1:p.Arg2598=
XM_011517555.2:c.7790G=	XP_011515857.1:p.Arg2597=
XM_017013612.1:c.7793G=	XP_016869101.1:p.Arg2598=
XM_017013613.1:c.7700G=	XP_016869102.1:p.Arg2567=
NM_017780.4:c.7703G= MANE Select	NP_060250.2:p.Arg2568=