Canonical Allele Identifier: CA2122506020

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429010G= , CM000676.2:g.21429010G=	GRCh38
NC_000014.8:g.21897169G= , CM000676.1:g.21897169G=	GRCh37
NC_000014.7:g.20967009G=	NCBI36
NG_021249.1:g.13289C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.332C=	ENSP00000406288.3:p.Pro111=
ENST00000553651.2:n.2975C=
ENST00000555962.6:c.-111+2801C=	ENSP00000495174.1:n.-111+2801C=
ENST00000557364.6:c.1169C=	ENSP00000451601.1:p.Pro390=
ENST00000642518.1:c.332C=	ENSP00000496722.1:p.Pro111=
ENST00000643048.1:n.1464C=
ENST00000643469.1:c.1169C=	ENSP00000495070.1:p.Pro390=
ENST00000645140.1:c.1081C=
ENST00000645929.1:c.332C=	ENSP00000494402.1:p.Pro111=
ENST00000646063.1:c.1256C=	ENSP00000496565.1:p.Pro419=
ENST00000646340.1:c.1175C=	ENSP00000496730.1:p.Pro392=
ENST00000646647.2:c.1169C= MANE Select	ENSP00000495240.1:p.Pro390=
ENST00000399982.6:c.1169C=	ENSP00000382863.2:p.Pro390=
ENST00000430710.7:c.332C=	ENSP00000406288.3:p.Pro111=
ENST00000555962.5:n.150+2801C=
ENST00000557364.5:c.1169C=	ENSP00000451601.1:p.Pro390=
NM_001170629.1:c.1169C=	NP_001164100.1:p.Pro390=
NM_020920.3:c.332C=	NP_065971.2:p.Pro111=
NM_001170629.2:c.1169C= MANE Select	NP_001164100.1:p.Pro390=
NM_020920.4:c.332C=	NP_065971.2:p.Pro111=