Canonical Allele Identifier: CA2122495173

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21401079G= , CM000676.2:g.21401079G=	GRCh38
NC_000014.8:g.21869238G= , CM000676.1:g.21869238G=	GRCh37
NC_000014.7:g.20939078G=	NCBI36
NG_021249.1:g.41220C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.3337-8C=	ENSP00000406288.3:n.3337-8C=
ENST00000555935.2:c.1850-8C=
ENST00000555962.6:c.265-772C=	ENSP00000495174.1:n.265-772C=
ENST00000557364.6:c.4174-8C=	ENSP00000451601.1:n.4174-8C=
ENST00000643469.1:c.4174-8C=	ENSP00000495070.1:n.4174-8C=
ENST00000645206.1:n.2688-8C=
ENST00000645929.1:c.3337-8C=	ENSP00000494402.1:n.3337-8C=
ENST00000646340.1:c.4180-8C=	ENSP00000496730.1:n.4180-8C=
ENST00000646558.1:n.728-8C=
ENST00000646647.2:c.4174-8C= MANE Select	ENSP00000495240.1:n.4174-8C=
ENST00000399982.6:c.4174-8C=	ENSP00000382863.2:n.4174-8C=
ENST00000430710.7:c.3337-8C=	ENSP00000406288.3:n.3337-8C=
ENST00000555935.1:c.1850-8C=
ENST00000555962.5:n.525-772C=
ENST00000557364.5:c.4174-8C=	ENSP00000451601.1:n.4174-8C=
NM_001170629.1:c.4174-8C=	NP_001164100.1:n.4174-8C=
NM_020920.3:c.3337-8C=	NP_065971.2:n.3337-8C=
NM_001170629.2:c.4174-8C= MANE Select	NP_001164100.1:n.4174-8C=
NM_020920.4:c.3337-8C=	NP_065971.2:n.3337-8C=