Canonical Allele Identifier: CA2122506087

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429071T= , CM000676.2:g.21429071T=	GRCh38
NC_000014.8:g.21897230T= , CM000676.1:g.21897230T=	GRCh37
NC_000014.7:g.20967070T=	NCBI36
NG_021249.1:g.13228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.271A=	ENSP00000406288.3:p.Thr91=
ENST00000553651.2:n.2914A=
ENST00000555962.6:c.-111+2740A=	ENSP00000495174.1:n.-111+2740A=
ENST00000557364.6:c.1108A=	ENSP00000451601.1:p.Thr370=
ENST00000642518.1:c.271A=	ENSP00000496722.1:p.Thr91=
ENST00000643048.1:n.1403A=
ENST00000643469.1:c.1108A=	ENSP00000495070.1:p.Thr370=
ENST00000645140.1:c.1020A=
ENST00000645929.1:c.271A=	ENSP00000494402.1:p.Thr91=
ENST00000646063.1:c.1195A=	ENSP00000496565.1:p.Thr399=
ENST00000646340.1:c.1114A=	ENSP00000496730.1:p.Thr372=
ENST00000646647.2:c.1108A= MANE Select	ENSP00000495240.1:p.Thr370=
ENST00000399982.6:c.1108A=	ENSP00000382863.2:p.Thr370=
ENST00000430710.7:c.271A=	ENSP00000406288.3:p.Thr91=
ENST00000555962.5:n.150+2740A=
ENST00000557364.5:c.1108A=	ENSP00000451601.1:p.Thr370=
NM_001170629.1:c.1108A=	NP_001164100.1:p.Thr370=
NM_020920.3:c.271A=	NP_065971.2:p.Thr91=
NM_001170629.2:c.1108A= MANE Select	NP_001164100.1:p.Thr370=
NM_020920.4:c.271A=	NP_065971.2:p.Thr91=