Canonical Allele Identifier: CA2122486736

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21394953G= , CM000676.2:g.21394953G=	GRCh38
NC_000014.8:g.21863112G= , CM000676.1:g.21863112G=	GRCh37
NC_000014.7:g.20932952G=	NCBI36
NG_021249.1:g.47346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.4512C=	ENSP00000406288.3:p.Ala1504=
ENST00000555935.2:c.3049C=
ENST00000555962.6:c.*734C=	ENSP00000495174.1:n.*734C=
ENST00000557364.6:c.5349C=	ENSP00000451601.1:p.Ala1783=
ENST00000643469.1:c.5349C=	ENSP00000495070.1:p.Ala1783=
ENST00000645206.1:n.4505C=
ENST00000645929.1:c.4512C=	ENSP00000494402.1:p.Ala1504=
ENST00000646340.1:c.5355C=	ENSP00000496730.1:p.Ala1785=
ENST00000646647.2:c.5349C= MANE Select	ENSP00000495240.1:p.Ala1783=
ENST00000399982.6:c.5349C=	ENSP00000382863.2:p.Ala1783=
ENST00000430710.7:c.4512C=	ENSP00000406288.3:p.Ala1504=
ENST00000555301.1:n.62C=
ENST00000557364.5:c.5349C=	ENSP00000451601.1:p.Ala1783=
NM_001170629.1:c.5349C=	NP_001164100.1:p.Ala1783=
NM_020920.3:c.4512C=	NP_065971.2:p.Ala1504=
NM_001170629.2:c.5349C= MANE Select	NP_001164100.1:p.Ala1783=
NM_020920.4:c.4512C=	NP_065971.2:p.Ala1504=