Canonical Allele Identifier: CA484992026

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897474G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429315G>T , CM000676.2:g.21429315G>T	GRCh38
NC_000014.8:g.21897474G>T , CM000676.1:g.21897474G>T	GRCh37
NC_000014.7:g.20967314G>T	NCBI36
NG_021249.1:g.12984C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.27C>A	ENSP00000406288.3:p.Thr9=
ENST00000553651.2:n.2670C>A
ENST00000555962.6:c.-111+2496C>A	ENSP00000495174.1:n.-111+2496C>A
ENST00000557364.6:c.864C>A	ENSP00000451601.1:p.Thr288=
ENST00000642518.1:c.27C>A	ENSP00000496722.1:p.Thr9=
ENST00000643048.1:n.1159C>A
ENST00000643469.1:c.864C>A	ENSP00000495070.1:p.Thr288=
ENST00000645140.1:c.776C>A
ENST00000645929.1:c.27C>A	ENSP00000494402.1:p.Thr9=
ENST00000646063.1:c.951C>A	ENSP00000496565.1:p.Thr317=
ENST00000646340.1:c.870C>A	ENSP00000496730.1:p.Thr290=
ENST00000646647.2:c.864C>A MANE Select	ENSP00000495240.1:p.Thr288=
ENST00000399982.6:c.864C>A	ENSP00000382863.2:p.Thr288=
ENST00000430710.7:c.27C>A	ENSP00000406288.3:p.Thr9=
ENST00000553283.1:c.117C>A	ENSP00000450860.1:p.Thr39=
ENST00000555962.5:n.150+2496C>A
ENST00000557364.5:c.864C>A	ENSP00000451601.1:p.Thr288=
NM_001170629.1:c.864C>A	NP_001164100.1:p.Thr288=
NM_020920.3:c.27C>A	NP_065971.2:p.Thr9=
NM_001170629.2:c.864C>A MANE Select	NP_001164100.1:p.Thr288=
NM_020920.4:c.27C>A	NP_065971.2:p.Thr9=