Canonical Allele Identifier: CA485000160

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21863187G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21395028G>A , CM000676.2:g.21395028G>A	GRCh38
NC_000014.8:g.21863187G>A , CM000676.1:g.21863187G>A	GRCh37
NC_000014.7:g.20933027G>A	NCBI36
NG_021249.1:g.47271C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.4437C>T	ENSP00000406288.3:p.Arg1479=
ENST00000555935.2:c.2974C>T
ENST00000555962.6:c.*659C>T	ENSP00000495174.1:n.*659C>T
ENST00000557364.6:c.5274C>T	ENSP00000451601.1:p.Arg1758=
ENST00000643469.1:c.5274C>T	ENSP00000495070.1:p.Arg1758=
ENST00000645206.1:n.4430C>T
ENST00000645929.1:c.4437C>T	ENSP00000494402.1:p.Arg1479=
ENST00000646340.1:c.5280C>T	ENSP00000496730.1:p.Arg1760=
ENST00000646647.2:c.5274C>T MANE Select	ENSP00000495240.1:p.Arg1758=
ENST00000399982.6:c.5274C>T	ENSP00000382863.2:p.Arg1758=
ENST00000430710.7:c.4437C>T	ENSP00000406288.3:p.Arg1479=
ENST00000555962.5:n.1228C>T
ENST00000557364.5:c.5274C>T	ENSP00000451601.1:p.Arg1758=
NM_001170629.1:c.5274C>T	NP_001164100.1:p.Arg1758=
NM_020920.3:c.4437C>T	NP_065971.2:p.Arg1479=
NM_001170629.2:c.5274C>T MANE Select	NP_001164100.1:p.Arg1758=
NM_020920.4:c.4437C>T	NP_065971.2:p.Arg1479=