Canonical Allele Identifier: CA388879950

Gene: CHD8

Linked Data

• ClinVar Variation Id: 2630872
• ClinVar RCV Id: RCV004550667
• MyVariant Identifiers: chr14:g.21861685C>T (hg19) ; chr14:g.21393526C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21393526C>T , CM000676.2:g.21393526C>T	GRCh38
NC_000014.8:g.21861685C>T , CM000676.1:g.21861685C>T	GRCh37
NC_000014.7:g.20931525C>T	NCBI36
NG_021249.1:g.48773G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.5432G>A	ENSP00000406288.3:p.Ser1811Asn
ENST00000555935.2:c.3969G>A
ENST00000557364.6:c.6269G>A	ENSP00000451601.1:p.Ser2090Asn
ENST00000643469.1:c.6269G>A	ENSP00000495070.1:p.Ser2090Asn
ENST00000645206.1:n.5425G>A
ENST00000645929.1:c.5432G>A	ENSP00000494402.1:p.Ser1811Asn
ENST00000646647.2:c.6269G>A MANE Select	ENSP00000495240.1:p.Ser2090Asn
ENST00000399982.6:c.6269G>A	ENSP00000382863.2:p.Ser2090Asn
ENST00000430710.7:c.5432G>A	ENSP00000406288.3:p.Ser1811Asn
ENST00000557364.5:c.6269G>A	ENSP00000451601.1:p.Ser2090Asn
NM_001170629.1:c.6269G>A	NP_001164100.1:p.Ser2090Asn
NM_020920.3:c.5432G>A	NP_065971.2:p.Ser1811Asn
NM_001170629.2:c.6269G>A MANE Select	NP_001164100.1:p.Ser2090Asn
NM_020920.4:c.5432G>A	NP_065971.2:p.Ser1811Asn