Canonical Allele Identifier: CA2122489865

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415885A= , CM000676.2:g.21415885A=	GRCh38
NC_000014.8:g.21884044A= , CM000676.1:g.21884044A=	GRCh37
NC_000014.7:g.20953884A=	NCBI36
NG_021249.1:g.26414T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.902T=	ENSP00000406288.3:p.Val301=
ENST00000555962.6:c.-110-12843T=	ENSP00000495174.1:n.-110-12843T=
ENST00000557364.6:c.1739T=	ENSP00000451601.1:p.Val580=
ENST00000642518.1:c.902T=	ENSP00000496722.1:p.Val301=
ENST00000642914.1:n.722T=
ENST00000643469.1:c.1739T=	ENSP00000495070.1:p.Val580=
ENST00000645140.1:c.1651T=
ENST00000645206.1:n.253T=
ENST00000645929.1:c.902T=	ENSP00000494402.1:p.Val301=
ENST00000646340.1:c.1745T=	ENSP00000496730.1:p.Val582=
ENST00000646647.2:c.1739T= MANE Select	ENSP00000495240.1:p.Val580=
ENST00000399982.6:c.1739T=	ENSP00000382863.2:p.Val580=
ENST00000430710.7:c.902T=	ENSP00000406288.3:p.Val301=
ENST00000555962.5:n.151-12843T=
ENST00000557364.5:c.1739T=	ENSP00000451601.1:p.Val580=
NM_001170629.1:c.1739T=	NP_001164100.1:p.Val580=
NM_020920.3:c.902T=	NP_065971.2:p.Val301=
NM_001170629.2:c.1739T= MANE Select	NP_001164100.1:p.Val580=
NM_020920.4:c.902T=	NP_065971.2:p.Val301=