Canonical Allele Identifier: CA2122503854

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21406961A= , CM000676.2:g.21406961A=	GRCh38
NC_000014.8:g.21875120A= , CM000676.1:g.21875120A=	GRCh37
NC_000014.7:g.20944960A=	NCBI36
NG_021249.1:g.35338T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1965T=	ENSP00000406288.3:p.Cys655=
ENST00000555935.2:c.478T=
ENST00000555962.6:c.-110-3919T=	ENSP00000495174.1:n.-110-3919T=
ENST00000557364.6:c.2802T=	ENSP00000451601.1:p.Cys934=
ENST00000643469.1:c.2802T=	ENSP00000495070.1:p.Cys934=
ENST00000645140.1:c.2714T=
ENST00000645206.1:n.1316T=
ENST00000645929.1:c.1965T=	ENSP00000494402.1:p.Cys655=
ENST00000646340.1:c.2808T=	ENSP00000496730.1:p.Cys936=
ENST00000646647.2:c.2802T= MANE Select	ENSP00000495240.1:p.Cys934=
ENST00000399982.6:c.2802T=	ENSP00000382863.2:p.Cys934=
ENST00000430710.7:c.1965T=	ENSP00000406288.3:p.Cys655=
ENST00000555935.1:c.478T=
ENST00000555962.5:n.151-3919T=
ENST00000557364.5:c.2802T=	ENSP00000451601.1:p.Cys934=
NM_001170629.1:c.2802T=	NP_001164100.1:p.Cys934=
NM_020920.3:c.1965T=	NP_065971.2:p.Cys655=
NM_001170629.2:c.2802T= MANE Select	NP_001164100.1:p.Cys934=
NM_020920.4:c.1965T=	NP_065971.2:p.Cys655=