Canonical Allele Identifier: CA2122502340

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21405764G= , CM000676.2:g.21405764G=	GRCh38
NC_000014.8:g.21873923G= , CM000676.1:g.21873923G=	GRCh37
NC_000014.7:g.20943763G=	NCBI36
NG_021249.1:g.36535C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.2171C=	ENSP00000406288.3:p.Ser724=
ENST00000555935.2:c.684C=
ENST00000555962.6:c.-110-2722C=	ENSP00000495174.1:n.-110-2722C=
ENST00000557364.6:c.3008C=	ENSP00000451601.1:p.Ser1003=
ENST00000643469.1:c.3008C=	ENSP00000495070.1:p.Ser1003=
ENST00000645140.1:c.2920C=
ENST00000645206.1:n.1522C=
ENST00000645929.1:c.2171C=	ENSP00000494402.1:p.Ser724=
ENST00000646340.1:c.3014C=	ENSP00000496730.1:p.Ser1005=
ENST00000646647.2:c.3008C= MANE Select	ENSP00000495240.1:p.Ser1003=
ENST00000399982.6:c.3008C=	ENSP00000382863.2:p.Ser1003=
ENST00000430710.7:c.2171C=	ENSP00000406288.3:p.Ser724=
ENST00000555935.1:c.684C=
ENST00000555962.5:n.151-2722C=
ENST00000557364.5:c.3008C=	ENSP00000451601.1:p.Ser1003=
NM_001170629.1:c.3008C=	NP_001164100.1:p.Ser1003=
NM_020920.3:c.2171C=	NP_065971.2:p.Ser724=
NM_001170629.2:c.3008C= MANE Select	NP_001164100.1:p.Ser1003=
NM_020920.4:c.2171C=	NP_065971.2:p.Ser724=