Canonical Allele Identifier: CA7091692

Gene: CHD8

Linked Data

• ClinVar Variation Id: 1949677
• ClinVar RCV Id: RCV002676400
• dbSNP Id: rs749068192
• ExAC: 14:21883876 C / T
• gnomAD v2: 14-21883876-C-T
• gnomAD v3: 14-21415717-C-T
• gnomAD v4: 14-21415717-C-T
• MyVariant Identifiers: chr14:g.21883876C>T (hg19) ; chr14:g.21415717C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415717C>T , CM000676.2:g.21415717C>T	GRCh38
NC_000014.8:g.21883876C>T , CM000676.1:g.21883876C>T	GRCh37
NC_000014.7:g.20953716C>T	NCBI36
NG_021249.1:g.26582G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1062+8G>A	ENSP00000406288.3:n.1062+8G>A
ENST00000555962.6:c.-110-12675G>A	ENSP00000495174.1:n.-110-12675G>A
ENST00000557364.6:c.1899+8G>A	ENSP00000451601.1:n.1899+8G>A
ENST00000642914.1:n.882+8G>A
ENST00000643469.1:c.1899+8G>A	ENSP00000495070.1:n.1899+8G>A
ENST00000645140.1:c.1811+8G>A
ENST00000645206.1:n.413+8G>A
ENST00000645929.1:c.1062+8G>A	ENSP00000494402.1:n.1062+8G>A
ENST00000646340.1:c.1905+8G>A	ENSP00000496730.1:n.1905+8G>A
ENST00000646647.2:c.1899+8G>A MANE Select	ENSP00000495240.1:n.1899+8G>A
ENST00000399982.6:c.1899+8G>A	ENSP00000382863.2:n.1899+8G>A
ENST00000430710.7:c.1062+8G>A	ENSP00000406288.3:n.1062+8G>A
ENST00000555962.5:n.151-12675G>A
ENST00000557364.5:c.1899+8G>A	ENSP00000451601.1:n.1899+8G>A
NM_001170629.1:c.1899+8G>A	NP_001164100.1:n.1899+8G>A
NM_020920.3:c.1062+8G>A	NP_065971.2:n.1062+8G>A
NM_001170629.2:c.1899+8G>A MANE Select	NP_001164100.1:n.1899+8G>A
NM_020920.4:c.1062+8G>A	NP_065971.2:n.1062+8G>A