Canonical Allele Identifier: CA2122483166

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21409851C= , CM000676.2:g.21409851C=	GRCh38
NC_000014.8:g.21878010C= , CM000676.1:g.21878010C=	GRCh37
NC_000014.7:g.20947850C=	NCBI36
NG_021249.1:g.32448G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.1527G=	ENSP00000406288.3:p.Val509=
ENST00000555935.2:c.40G=
ENST00000555962.6:c.-110-6809G=	ENSP00000495174.1:n.-110-6809G=
ENST00000557364.6:c.2364G=	ENSP00000451601.1:p.Val788=
ENST00000643469.1:c.2364G=	ENSP00000495070.1:p.Val788=
ENST00000645140.1:c.2276G=
ENST00000645206.1:n.878G=
ENST00000645929.1:c.1527G=	ENSP00000494402.1:p.Val509=
ENST00000646340.1:c.2370G=	ENSP00000496730.1:p.Val790=
ENST00000646647.2:c.2364G= MANE Select	ENSP00000495240.1:p.Val788=
ENST00000399982.6:c.2364G=	ENSP00000382863.2:p.Val788=
ENST00000430710.7:c.1527G=	ENSP00000406288.3:p.Val509=
ENST00000554384.1:n.232G=
ENST00000555935.1:c.40G=
ENST00000555962.5:n.151-6809G=
ENST00000557364.5:c.2364G=	ENSP00000451601.1:p.Val788=
NM_001170629.1:c.2364G=	NP_001164100.1:p.Val788=
NM_020920.3:c.1527G=	NP_065971.2:p.Val509=
NM_001170629.2:c.2364G= MANE Select	NP_001164100.1:p.Val788=
NM_020920.4:c.1527G=	NP_065971.2:p.Val509=