Canonical Allele Identifier: CA2580087818

Gene: CHD8

Linked Data

• ClinVar Variation Id: 2016286
• ClinVar RCV Id: RCV002851499
• gnomAD v4: 14-21415653-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415653A>C , CM000676.2:g.21415653A>C	GRCh38
NC_000014.8:g.21883812A>C , CM000676.1:g.21883812A>C	GRCh37
NC_000014.7:g.20953652A>C	NCBI36
NG_021249.1:g.26646T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1063-11T>G	ENSP00000406288.3:n.1063-11T>G
ENST00000555962.6:c.-110-12611T>G	ENSP00000495174.1:n.-110-12611T>G
ENST00000557364.6:c.1900-11T>G	ENSP00000451601.1:n.1900-11T>G
ENST00000642914.1:n.883-11T>G
ENST00000643469.1:c.1900-11T>G	ENSP00000495070.1:n.1900-11T>G
ENST00000645140.1:c.1812-11T>G
ENST00000645206.1:n.414-11T>G
ENST00000645929.1:c.1063-11T>G	ENSP00000494402.1:n.1063-11T>G
ENST00000646340.1:c.1906-11T>G	ENSP00000496730.1:n.1906-11T>G
ENST00000646647.2:c.1900-11T>G MANE Select	ENSP00000495240.1:n.1900-11T>G
ENST00000399982.6:c.1900-11T>G	ENSP00000382863.2:n.1900-11T>G
ENST00000430710.7:c.1063-11T>G	ENSP00000406288.3:n.1063-11T>G
ENST00000555962.5:n.151-12611T>G
ENST00000557364.5:c.1900-11T>G	ENSP00000451601.1:n.1900-11T>G
NM_001170629.1:c.1900-11T>G	NP_001164100.1:n.1900-11T>G
NM_020920.3:c.1063-11T>G	NP_065971.2:n.1063-11T>G
NM_001170629.2:c.1900-11T>G MANE Select	NP_001164100.1:n.1900-11T>G
NM_020920.4:c.1063-11T>G	NP_065971.2:n.1063-11T>G