Canonical Allele Identifier: CA484987327

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21884039G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415880G>T , CM000676.2:g.21415880G>T	GRCh38
NC_000014.8:g.21884039G>T , CM000676.1:g.21884039G>T	GRCh37
NC_000014.7:g.20953879G>T	NCBI36
NG_021249.1:g.26419C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.907C>A	ENSP00000406288.3:p.Arg303=
ENST00000555962.6:c.-110-12838C>A	ENSP00000495174.1:n.-110-12838C>A
ENST00000557364.6:c.1744C>A	ENSP00000451601.1:p.Arg582=
ENST00000642518.1:c.907C>A	ENSP00000496722.1:p.Arg303=
ENST00000642914.1:n.727C>A
ENST00000643469.1:c.1744C>A	ENSP00000495070.1:p.Arg582=
ENST00000645140.1:c.1656C>A
ENST00000645206.1:n.258C>A
ENST00000645929.1:c.907C>A	ENSP00000494402.1:p.Arg303=
ENST00000646340.1:c.1750C>A	ENSP00000496730.1:p.Arg584=
ENST00000646647.2:c.1744C>A MANE Select	ENSP00000495240.1:p.Arg582=
ENST00000399982.6:c.1744C>A	ENSP00000382863.2:p.Arg582=
ENST00000430710.7:c.907C>A	ENSP00000406288.3:p.Arg303=
ENST00000555962.5:n.151-12838C>A
ENST00000557364.5:c.1744C>A	ENSP00000451601.1:p.Arg582=
NM_001170629.1:c.1744C>A	NP_001164100.1:p.Arg582=
NM_020920.3:c.907C>A	NP_065971.2:p.Arg303=
NM_001170629.2:c.1744C>A MANE Select	NP_001164100.1:p.Arg582=
NM_020920.4:c.907C>A	NP_065971.2:p.Arg303=