Canonical Allele Identifier: CA484991403

Gene: CHD8

Linked Data

• dbSNP Id: rs1265205771
• gnomAD v2: 14-21897198-C-T
• gnomAD v4: 14-21429039-C-T
• MyVariant Identifiers: chr14:g.21897198C>T (hg19) ; chr14:g.21429039C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429039C>T , CM000676.2:g.21429039C>T	GRCh38
NC_000014.8:g.21897198C>T , CM000676.1:g.21897198C>T	GRCh37
NC_000014.7:g.20967038C>T	NCBI36
NG_021249.1:g.13260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.303G>A	ENSP00000406288.3:p.Gln101=
ENST00000553651.2:n.2946G>A
ENST00000555962.6:c.-111+2772G>A	ENSP00000495174.1:n.-111+2772G>A
ENST00000557364.6:c.1140G>A	ENSP00000451601.1:p.Gln380=
ENST00000642518.1:c.303G>A	ENSP00000496722.1:p.Gln101=
ENST00000643048.1:n.1435G>A
ENST00000643469.1:c.1140G>A	ENSP00000495070.1:p.Gln380=
ENST00000645140.1:c.1052G>A
ENST00000645929.1:c.303G>A	ENSP00000494402.1:p.Gln101=
ENST00000646063.1:c.1227G>A	ENSP00000496565.1:p.Gln409=
ENST00000646340.1:c.1146G>A	ENSP00000496730.1:p.Gln382=
ENST00000646647.2:c.1140G>A MANE Select	ENSP00000495240.1:p.Gln380=
ENST00000399982.6:c.1140G>A	ENSP00000382863.2:p.Gln380=
ENST00000430710.7:c.303G>A	ENSP00000406288.3:p.Gln101=
ENST00000555962.5:n.150+2772G>A
ENST00000557364.5:c.1140G>A	ENSP00000451601.1:p.Gln380=
NM_001170629.1:c.1140G>A	NP_001164100.1:p.Gln380=
NM_020920.3:c.303G>A	NP_065971.2:p.Gln101=
NM_001170629.2:c.1140G>A MANE Select	NP_001164100.1:p.Gln380=
NM_020920.4:c.303G>A	NP_065971.2:p.Gln101=