Canonical Allele Identifier: CA388885735

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897475G>A (hg19) ; chr14:g.21429316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429316G>A , CM000676.2:g.21429316G>A	GRCh38
NC_000014.8:g.21897475G>A , CM000676.1:g.21897475G>A	GRCh37
NC_000014.7:g.20967315G>A	NCBI36
NG_021249.1:g.12983C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.26C>T	ENSP00000406288.3:p.Thr9Ile
ENST00000553651.2:n.2669C>T
ENST00000555962.6:c.-111+2495C>T	ENSP00000495174.1:n.-111+2495C>T
ENST00000557364.6:c.863C>T	ENSP00000451601.1:p.Thr288Ile
ENST00000642518.1:c.26C>T	ENSP00000496722.1:p.Thr9Ile
ENST00000643048.1:n.1158C>T
ENST00000643469.1:c.863C>T	ENSP00000495070.1:p.Thr288Ile
ENST00000645140.1:c.775C>T
ENST00000645929.1:c.26C>T	ENSP00000494402.1:p.Thr9Ile
ENST00000646063.1:c.950C>T	ENSP00000496565.1:p.Thr317Ile
ENST00000646340.1:c.869C>T	ENSP00000496730.1:p.Thr290Ile
ENST00000646647.2:c.863C>T MANE Select	ENSP00000495240.1:p.Thr288Ile
ENST00000399982.6:c.863C>T	ENSP00000382863.2:p.Thr288Ile
ENST00000430710.7:c.26C>T	ENSP00000406288.3:p.Thr9Ile
ENST00000553283.1:c.116C>T	ENSP00000450860.1:p.Thr39Ile
ENST00000555962.5:n.150+2495C>T
ENST00000557364.5:c.863C>T	ENSP00000451601.1:p.Thr288Ile
NM_001170629.1:c.863C>T	NP_001164100.1:p.Thr288Ile
NM_020920.3:c.26C>T	NP_065971.2:p.Thr9Ile
NM_001170629.2:c.863C>T MANE Select	NP_001164100.1:p.Thr288Ile
NM_020920.4:c.26C>T	NP_065971.2:p.Thr9Ile