Canonical Allele Identifier: CA388880220

Gene: CHD8

Linked Data

• gnomAD v4: 14-21393601-T-A
• MyVariant Identifiers: chr14:g.21861760T>A (hg19) ; chr14:g.21393601T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21393601T>A , CM000676.2:g.21393601T>A	GRCh38
NC_000014.8:g.21861760T>A , CM000676.1:g.21861760T>A	GRCh37
NC_000014.7:g.20931600T>A	NCBI36
NG_021249.1:g.48698A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.5357A>T	ENSP00000406288.3:p.Asp1786Val
ENST00000555935.2:c.3894A>T
ENST00000557364.6:c.6194A>T	ENSP00000451601.1:p.Asp2065Val
ENST00000643469.1:c.6194A>T	ENSP00000495070.1:p.Asp2065Val
ENST00000645206.1:n.5350A>T
ENST00000645929.1:c.5357A>T	ENSP00000494402.1:p.Asp1786Val
ENST00000646647.2:c.6194A>T MANE Select	ENSP00000495240.1:p.Asp2065Val
ENST00000399982.6:c.6194A>T	ENSP00000382863.2:p.Asp2065Val
ENST00000430710.7:c.5357A>T	ENSP00000406288.3:p.Asp1786Val
ENST00000557364.5:c.6194A>T	ENSP00000451601.1:p.Asp2065Val
NM_001170629.1:c.6194A>T	NP_001164100.1:p.Asp2065Val
NM_020920.3:c.5357A>T	NP_065971.2:p.Asp1786Val
NM_001170629.2:c.6194A>T MANE Select	NP_001164100.1:p.Asp2065Val
NM_020920.4:c.5357A>T	NP_065971.2:p.Asp1786Val