Canonical Allele Identifier: CA388884220

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21863233G>T (hg19) ; chr14:g.21395074G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21395074G>T , CM000676.2:g.21395074G>T	GRCh38
NC_000014.8:g.21863233G>T , CM000676.1:g.21863233G>T	GRCh37
NC_000014.7:g.20933073G>T	NCBI36
NG_021249.1:g.47225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.4391C>A	ENSP00000406288.3:p.Ser1464Tyr
ENST00000555935.2:c.2928C>A
ENST00000555962.6:c.*613C>A	ENSP00000495174.1:n.*613C>A
ENST00000557364.6:c.5228C>A	ENSP00000451601.1:p.Ser1743Tyr
ENST00000643469.1:c.5228C>A	ENSP00000495070.1:p.Ser1743Tyr
ENST00000645206.1:n.4384C>A
ENST00000645929.1:c.4391C>A	ENSP00000494402.1:p.Ser1464Tyr
ENST00000646340.1:c.5234C>A	ENSP00000496730.1:p.Ser1745Tyr
ENST00000646647.2:c.5228C>A MANE Select	ENSP00000495240.1:p.Ser1743Tyr
ENST00000399982.6:c.5228C>A	ENSP00000382863.2:p.Ser1743Tyr
ENST00000430710.7:c.4391C>A	ENSP00000406288.3:p.Ser1464Tyr
ENST00000555962.5:n.1182C>A
ENST00000557364.5:c.5228C>A	ENSP00000451601.1:p.Ser1743Tyr
NM_001170629.1:c.5228C>A	NP_001164100.1:p.Ser1743Tyr
NM_020920.3:c.4391C>A	NP_065971.2:p.Ser1464Tyr
NM_001170629.2:c.5228C>A MANE Select	NP_001164100.1:p.Ser1743Tyr
NM_020920.4:c.4391C>A	NP_065971.2:p.Ser1464Tyr