Canonical Allele Identifier: CA388885825

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897494C>A (hg19) ; chr14:g.21429335C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429335C>A , CM000676.2:g.21429335C>A	GRCh38
NC_000014.8:g.21897494C>A , CM000676.1:g.21897494C>A	GRCh37
NC_000014.7:g.20967334C>A	NCBI36
NG_021249.1:g.12964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.7G>T	ENSP00000406288.3:p.Gly3Cys
ENST00000553651.2:n.2650G>T
ENST00000555962.6:c.-111+2476G>T	ENSP00000495174.1:n.-111+2476G>T
ENST00000557364.6:c.844G>T	ENSP00000451601.1:p.Gly282Cys
ENST00000642518.1:c.7G>T	ENSP00000496722.1:p.Gly3Cys
ENST00000643048.1:n.1139G>T
ENST00000643469.1:c.844G>T	ENSP00000495070.1:p.Gly282Cys
ENST00000645140.1:c.756G>T
ENST00000645929.1:c.7G>T	ENSP00000494402.1:p.Gly3Cys
ENST00000646063.1:c.931G>T	ENSP00000496565.1:p.Gly311Cys
ENST00000646340.1:c.850G>T	ENSP00000496730.1:p.Gly284Cys
ENST00000646647.2:c.844G>T MANE Select	ENSP00000495240.1:p.Gly282Cys
ENST00000399982.6:c.844G>T	ENSP00000382863.2:p.Gly282Cys
ENST00000430710.7:c.7G>T	ENSP00000406288.3:p.Gly3Cys
ENST00000553283.1:c.97G>T	ENSP00000450860.1:p.Gly33Cys
ENST00000555962.5:n.150+2476G>T
ENST00000557364.5:c.844G>T	ENSP00000451601.1:p.Gly282Cys
NM_001170629.1:c.844G>T	NP_001164100.1:p.Gly282Cys
NM_020920.3:c.7G>T	NP_065971.2:p.Gly3Cys
NM_001170629.2:c.844G>T MANE Select	NP_001164100.1:p.Gly282Cys
NM_020920.4:c.7G>T	NP_065971.2:p.Gly3Cys