Canonical Allele Identifier: CA16619833

Gene: CHD8

Linked Data

• ClinVar Variation Id: 419510
• ClinVar RCV Id: RCV000482586 ; RCV002526547 ; RCV003409656
• dbSNP Id: rs991738444
• gnomAD v4: 14-21400569-G-A
• COSMIC: COSM954430 ; COSM1587316
• MyVariant Identifiers: chr14:g.21868728G>A (hg19) ; chr14:g.21400569G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21400569G>A , CM000676.2:g.21400569G>A	GRCh38
NC_000014.8:g.21868728G>A , CM000676.1:g.21868728G>A	GRCh37
NC_000014.7:g.20938568G>A	NCBI36
NG_021249.1:g.41730C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.3577C>T	ENSP00000406288.3:p.Arg1193Ter
ENST00000555935.2:c.2090C>T
ENST00000555962.6:c.265-262C>T	ENSP00000495174.1:n.265-262C>T
ENST00000557364.6:c.4414C>T	ENSP00000451601.1:p.Arg1472Ter
ENST00000643469.1:c.4414C>T	ENSP00000495070.1:p.Arg1472Ter
ENST00000645206.1:n.2928C>T
ENST00000645929.1:c.3577C>T	ENSP00000494402.1:p.Arg1193Ter
ENST00000646340.1:c.4420C>T	ENSP00000496730.1:p.Arg1474Ter
ENST00000646558.1:n.1230C>T
ENST00000646647.2:c.4414C>T MANE Select	ENSP00000495240.1:p.Arg1472Ter
ENST00000399982.6:c.4414C>T	ENSP00000382863.2:p.Arg1472Ter
ENST00000430710.7:c.3577C>T	ENSP00000406288.3:p.Arg1193Ter
ENST00000555935.1:c.2090C>T
ENST00000555962.5:n.525-262C>T
ENST00000557364.5:c.4414C>T	ENSP00000451601.1:p.Arg1472Ter
NM_001170629.1:c.4414C>T	NP_001164100.1:p.Arg1472Ter
NM_020920.3:c.3577C>T	NP_065971.2:p.Arg1193Ter
NM_001170629.2:c.4414C>T MANE Select	NP_001164100.1:p.Arg1472Ter
NM_020920.4:c.3577C>T	NP_065971.2:p.Arg1193Ter