Canonical Allele Identifier: CA388884020

Gene: CHD8

Linked Data

• gnomAD v4: 14-21394982-C-A
• MyVariant Identifiers: chr14:g.21863141C>A (hg19) ; chr14:g.21394982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21394982C>A , CM000676.2:g.21394982C>A	GRCh38
NC_000014.8:g.21863141C>A , CM000676.1:g.21863141C>A	GRCh37
NC_000014.7:g.20932981C>A	NCBI36
NG_021249.1:g.47317G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.4483G>T	ENSP00000406288.3:p.Asp1495Tyr
ENST00000555935.2:c.3020G>T
ENST00000555962.6:c.*705G>T	ENSP00000495174.1:n.*705G>T
ENST00000557364.6:c.5320G>T	ENSP00000451601.1:p.Asp1774Tyr
ENST00000643469.1:c.5320G>T	ENSP00000495070.1:p.Asp1774Tyr
ENST00000645206.1:n.4476G>T
ENST00000645929.1:c.4483G>T	ENSP00000494402.1:p.Asp1495Tyr
ENST00000646340.1:c.5326G>T	ENSP00000496730.1:p.Asp1776Tyr
ENST00000646647.2:c.5320G>T MANE Select	ENSP00000495240.1:p.Asp1774Tyr
ENST00000399982.6:c.5320G>T	ENSP00000382863.2:p.Asp1774Tyr
ENST00000430710.7:c.4483G>T	ENSP00000406288.3:p.Asp1495Tyr
ENST00000555301.1:n.33G>T
ENST00000557364.5:c.5320G>T	ENSP00000451601.1:p.Asp1774Tyr
NM_001170629.1:c.5320G>T	NP_001164100.1:p.Asp1774Tyr
NM_020920.3:c.4483G>T	NP_065971.2:p.Asp1495Tyr
NM_001170629.2:c.5320G>T MANE Select	NP_001164100.1:p.Asp1774Tyr
NM_020920.4:c.4483G>T	NP_065971.2:p.Asp1495Tyr