Canonical Allele Identifier: CA2122506144

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21393676T= , CM000676.2:g.21393676T=	GRCh38
NC_000014.8:g.21861835T= , CM000676.1:g.21861835T=	GRCh37
NC_000014.7:g.20931675T=	NCBI36
NG_021249.1:g.48623A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.5282A=	ENSP00000406288.3:p.Asp1761=
ENST00000555935.2:c.3819A=
ENST00000557364.6:c.6119A=	ENSP00000451601.1:p.Asp2040=
ENST00000643469.1:c.6119A=	ENSP00000495070.1:p.Asp2040=
ENST00000645206.1:n.5275A=
ENST00000645929.1:c.5282A=	ENSP00000494402.1:p.Asp1761=
ENST00000646647.2:c.6119A= MANE Select	ENSP00000495240.1:p.Asp2040=
ENST00000399982.6:c.6119A=	ENSP00000382863.2:p.Asp2040=
ENST00000430710.7:c.5282A=	ENSP00000406288.3:p.Asp1761=
ENST00000555301.1:n.913A=
ENST00000557364.5:c.6119A=	ENSP00000451601.1:p.Asp2040=
NM_001170629.1:c.6119A=	NP_001164100.1:p.Asp2040=
NM_020920.3:c.5282A=	NP_065971.2:p.Asp1761=
NM_001170629.2:c.6119A= MANE Select	NP_001164100.1:p.Asp2040=
NM_020920.4:c.5282A=	NP_065971.2:p.Asp1761=