Canonical Allele Identifier: CA388884341

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897125G>T (hg19) ; chr14:g.21428966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21428966G>T , CM000676.2:g.21428966G>T	GRCh38
NC_000014.8:g.21897125G>T , CM000676.1:g.21897125G>T	GRCh37
NC_000014.7:g.20966965G>T	NCBI36
NG_021249.1:g.13333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.376C>A	ENSP00000406288.3:p.Gln126Lys
ENST00000553651.2:n.3019C>A
ENST00000555962.6:c.-111+2845C>A	ENSP00000495174.1:n.-111+2845C>A
ENST00000557364.6:c.1213C>A	ENSP00000451601.1:p.Gln405Lys
ENST00000642518.1:c.376C>A	ENSP00000496722.1:p.Gln126Lys
ENST00000643048.1:n.1508C>A
ENST00000643469.1:c.1213C>A	ENSP00000495070.1:p.Gln405Lys
ENST00000645140.1:c.1125C>A
ENST00000645929.1:c.376C>A	ENSP00000494402.1:p.Gln126Lys
ENST00000646063.1:c.1300C>A	ENSP00000496565.1:p.Gln434Lys
ENST00000646340.1:c.1219C>A	ENSP00000496730.1:p.Gln407Lys
ENST00000646647.2:c.1213C>A MANE Select	ENSP00000495240.1:p.Gln405Lys
ENST00000399982.6:c.1213C>A	ENSP00000382863.2:p.Gln405Lys
ENST00000430710.7:c.376C>A	ENSP00000406288.3:p.Gln126Lys
ENST00000555962.5:n.150+2845C>A
ENST00000557364.5:c.1213C>A	ENSP00000451601.1:p.Gln405Lys
NM_001170629.1:c.1213C>A	NP_001164100.1:p.Gln405Lys
NM_020920.3:c.376C>A	NP_065971.2:p.Gln126Lys
NM_001170629.2:c.1213C>A MANE Select	NP_001164100.1:p.Gln405Lys
NM_020920.4:c.376C>A	NP_065971.2:p.Gln126Lys