Canonical Allele Identifier: CA388884499

Gene: CHD8

Linked Data

• gnomAD v4: 14-21429008-C-T
• MyVariant Identifiers: chr14:g.21897167C>T (hg19) ; chr14:g.21429008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429008C>T , CM000676.2:g.21429008C>T	GRCh38
NC_000014.8:g.21897167C>T , CM000676.1:g.21897167C>T	GRCh37
NC_000014.7:g.20967007C>T	NCBI36
NG_021249.1:g.13291G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.334G>A	ENSP00000406288.3:p.Gly112Arg
ENST00000553651.2:n.2977G>A
ENST00000555962.6:c.-111+2803G>A	ENSP00000495174.1:n.-111+2803G>A
ENST00000557364.6:c.1171G>A	ENSP00000451601.1:p.Gly391Arg
ENST00000642518.1:c.334G>A	ENSP00000496722.1:p.Gly112Arg
ENST00000643048.1:n.1466G>A
ENST00000643469.1:c.1171G>A	ENSP00000495070.1:p.Gly391Arg
ENST00000645140.1:c.1083G>A
ENST00000645929.1:c.334G>A	ENSP00000494402.1:p.Gly112Arg
ENST00000646063.1:c.1258G>A	ENSP00000496565.1:p.Gly420Arg
ENST00000646340.1:c.1177G>A	ENSP00000496730.1:p.Gly393Arg
ENST00000646647.2:c.1171G>A MANE Select	ENSP00000495240.1:p.Gly391Arg
ENST00000399982.6:c.1171G>A	ENSP00000382863.2:p.Gly391Arg
ENST00000430710.7:c.334G>A	ENSP00000406288.3:p.Gly112Arg
ENST00000555962.5:n.150+2803G>A
ENST00000557364.5:c.1171G>A	ENSP00000451601.1:p.Gly391Arg
NM_001170629.1:c.1171G>A	NP_001164100.1:p.Gly391Arg
NM_020920.3:c.334G>A	NP_065971.2:p.Gly112Arg
NM_001170629.2:c.1171G>A MANE Select	NP_001164100.1:p.Gly391Arg
NM_020920.4:c.334G>A	NP_065971.2:p.Gly112Arg