Canonical Allele Identifier: CA388879201

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21883770A>C (hg19) ; chr14:g.21415611A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415611A>C , CM000676.2:g.21415611A>C	GRCh38
NC_000014.8:g.21883770A>C , CM000676.1:g.21883770A>C	GRCh37
NC_000014.7:g.20953610A>C	NCBI36
NG_021249.1:g.26688T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1094T>G	ENSP00000406288.3:p.Val365Gly
ENST00000555962.6:c.-110-12569T>G	ENSP00000495174.1:n.-110-12569T>G
ENST00000557364.6:c.1931T>G	ENSP00000451601.1:p.Val644Gly
ENST00000642914.1:n.914T>G
ENST00000643469.1:c.1931T>G	ENSP00000495070.1:p.Val644Gly
ENST00000645140.1:c.1843T>G
ENST00000645206.1:n.445T>G
ENST00000645929.1:c.1094T>G	ENSP00000494402.1:p.Val365Gly
ENST00000646340.1:c.1937T>G	ENSP00000496730.1:p.Val646Gly
ENST00000646647.2:c.1931T>G MANE Select	ENSP00000495240.1:p.Val644Gly
ENST00000399982.6:c.1931T>G	ENSP00000382863.2:p.Val644Gly
ENST00000430710.7:c.1094T>G	ENSP00000406288.3:p.Val365Gly
ENST00000555962.5:n.151-12569T>G
ENST00000557364.5:c.1931T>G	ENSP00000451601.1:p.Val644Gly
NM_001170629.1:c.1931T>G	NP_001164100.1:p.Val644Gly
NM_020920.3:c.1094T>G	NP_065971.2:p.Val365Gly
NM_001170629.2:c.1931T>G MANE Select	NP_001164100.1:p.Val644Gly
NM_020920.4:c.1094T>G	NP_065971.2:p.Val365Gly