Canonical Allele Identifier: CA388879221

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21883774T>C (hg19) ; chr14:g.21415615T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415615T>C , CM000676.2:g.21415615T>C	GRCh38
NC_000014.8:g.21883774T>C , CM000676.1:g.21883774T>C	GRCh37
NC_000014.7:g.20953614T>C	NCBI36
NG_021249.1:g.26684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1090A>G	ENSP00000406288.3:p.Ile364Val
ENST00000555962.6:c.-110-12573A>G	ENSP00000495174.1:n.-110-12573A>G
ENST00000557364.6:c.1927A>G	ENSP00000451601.1:p.Ile643Val
ENST00000642914.1:n.910A>G
ENST00000643469.1:c.1927A>G	ENSP00000495070.1:p.Ile643Val
ENST00000645140.1:c.1839A>G
ENST00000645206.1:n.441A>G
ENST00000645929.1:c.1090A>G	ENSP00000494402.1:p.Ile364Val
ENST00000646340.1:c.1933A>G	ENSP00000496730.1:p.Ile645Val
ENST00000646647.2:c.1927A>G MANE Select	ENSP00000495240.1:p.Ile643Val
ENST00000399982.6:c.1927A>G	ENSP00000382863.2:p.Ile643Val
ENST00000430710.7:c.1090A>G	ENSP00000406288.3:p.Ile364Val
ENST00000555962.5:n.151-12573A>G
ENST00000557364.5:c.1927A>G	ENSP00000451601.1:p.Ile643Val
NM_001170629.1:c.1927A>G	NP_001164100.1:p.Ile643Val
NM_020920.3:c.1090A>G	NP_065971.2:p.Ile364Val
NM_001170629.2:c.1927A>G MANE Select	NP_001164100.1:p.Ile643Val
NM_020920.4:c.1090A>G	NP_065971.2:p.Ile364Val