Canonical Allele Identifier: CA2122506053

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429026C= , CM000676.2:g.21429026C=	GRCh38
NC_000014.8:g.21897185C= , CM000676.1:g.21897185C=	GRCh37
NC_000014.7:g.20967025C=	NCBI36
NG_021249.1:g.13273G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.316G=	ENSP00000406288.3:p.Gly106=
ENST00000553651.2:n.2959G=
ENST00000555962.6:c.-111+2785G=	ENSP00000495174.1:n.-111+2785G=
ENST00000557364.6:c.1153G=	ENSP00000451601.1:p.Gly385=
ENST00000642518.1:c.316G=	ENSP00000496722.1:p.Gly106=
ENST00000643048.1:n.1448G=
ENST00000643469.1:c.1153G=	ENSP00000495070.1:p.Gly385=
ENST00000645140.1:c.1065G=
ENST00000645929.1:c.316G=	ENSP00000494402.1:p.Gly106=
ENST00000646063.1:c.1240G=	ENSP00000496565.1:p.Gly414=
ENST00000646340.1:c.1159G=	ENSP00000496730.1:p.Gly387=
ENST00000646647.2:c.1153G= MANE Select	ENSP00000495240.1:p.Gly385=
ENST00000399982.6:c.1153G=	ENSP00000382863.2:p.Gly385=
ENST00000430710.7:c.316G=	ENSP00000406288.3:p.Gly106=
ENST00000555962.5:n.150+2785G=
ENST00000557364.5:c.1153G=	ENSP00000451601.1:p.Gly385=
NM_001170629.1:c.1153G=	NP_001164100.1:p.Gly385=
NM_020920.3:c.316G=	NP_065971.2:p.Gly106=
NM_001170629.2:c.1153G= MANE Select	NP_001164100.1:p.Gly385=
NM_020920.4:c.316G=	NP_065971.2:p.Gly106=