Canonical Allele Identifier: CA388880664

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21861982G>C (hg19) ; chr14:g.21393823G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21393823G>C , CM000676.2:g.21393823G>C	GRCh38
NC_000014.8:g.21861982G>C , CM000676.1:g.21861982G>C	GRCh37
NC_000014.7:g.20931822G>C	NCBI36
NG_021249.1:g.48476C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.5135C>G	ENSP00000406288.3:p.Ser1712Ter
ENST00000555935.2:c.3672C>G
ENST00000557364.6:c.5972C>G	ENSP00000451601.1:p.Ser1991Ter
ENST00000643469.1:c.5972C>G	ENSP00000495070.1:p.Ser1991Ter
ENST00000645206.1:n.5128C>G
ENST00000645929.1:c.5135C>G	ENSP00000494402.1:p.Ser1712Ter
ENST00000646340.1:c.5978C>G	ENSP00000496730.1:p.Ser1993Ter
ENST00000646647.2:c.5972C>G MANE Select	ENSP00000495240.1:p.Ser1991Ter
ENST00000399982.6:c.5972C>G	ENSP00000382863.2:p.Ser1991Ter
ENST00000430710.7:c.5135C>G	ENSP00000406288.3:p.Ser1712Ter
ENST00000555301.1:n.766C>G
ENST00000557364.5:c.5972C>G	ENSP00000451601.1:p.Ser1991Ter
NM_001170629.1:c.5972C>G	NP_001164100.1:p.Ser1991Ter
NM_020920.3:c.5135C>G	NP_065971.2:p.Ser1712Ter
NM_001170629.2:c.5972C>G MANE Select	NP_001164100.1:p.Ser1991Ter
NM_020920.4:c.5135C>G	NP_065971.2:p.Ser1712Ter