Canonical Allele Identifier: CA388885187

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897339C>G (hg19) ; chr14:g.21429180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429180C>G , CM000676.2:g.21429180C>G	GRCh38
NC_000014.8:g.21897339C>G , CM000676.1:g.21897339C>G	GRCh37
NC_000014.7:g.20967179C>G	NCBI36
NG_021249.1:g.13119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.162G>C	ENSP00000406288.3:p.Gln54His
ENST00000553651.2:n.2805G>C
ENST00000555962.6:c.-111+2631G>C	ENSP00000495174.1:n.-111+2631G>C
ENST00000557364.6:c.999G>C	ENSP00000451601.1:p.Gln333His
ENST00000642518.1:c.162G>C	ENSP00000496722.1:p.Gln54His
ENST00000643048.1:n.1294G>C
ENST00000643469.1:c.999G>C	ENSP00000495070.1:p.Gln333His
ENST00000645140.1:c.911G>C
ENST00000645929.1:c.162G>C	ENSP00000494402.1:p.Gln54His
ENST00000646063.1:c.1086G>C	ENSP00000496565.1:p.Gln362His
ENST00000646340.1:c.1005G>C	ENSP00000496730.1:p.Gln335His
ENST00000646647.2:c.999G>C MANE Select	ENSP00000495240.1:p.Gln333His
ENST00000399982.6:c.999G>C	ENSP00000382863.2:p.Gln333His
ENST00000430710.7:c.162G>C	ENSP00000406288.3:p.Gln54His
ENST00000553283.1:c.252G>C	ENSP00000450860.1:p.Gln84His
ENST00000555962.5:n.150+2631G>C
ENST00000557364.5:c.999G>C	ENSP00000451601.1:p.Gln333His
NM_001170629.1:c.999G>C	NP_001164100.1:p.Gln333His
NM_020920.3:c.162G>C	NP_065971.2:p.Gln54His
NM_001170629.2:c.999G>C MANE Select	NP_001164100.1:p.Gln333His
NM_020920.4:c.162G>C	NP_065971.2:p.Gln54His