Canonical Allele Identifier: CA388879119

Gene: CHD8

Linked Data

• ClinVar Variation Id: 1213586
• ClinVar RCV Id: RCV001581735
• dbSNP Id: rs1329659775
• gnomAD v4: 14-21415591-G-A
• MyVariant Identifiers: chr14:g.21883750G>A (hg19) ; chr14:g.21415591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415591G>A , CM000676.2:g.21415591G>A	GRCh38
NC_000014.8:g.21883750G>A , CM000676.1:g.21883750G>A	GRCh37
NC_000014.7:g.20953590G>A	NCBI36
NG_021249.1:g.26708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1114C>T	ENSP00000406288.3:p.Arg372Trp
ENST00000555962.6:c.-110-12549C>T	ENSP00000495174.1:n.-110-12549C>T
ENST00000557364.6:c.1951C>T	ENSP00000451601.1:p.Arg651Trp
ENST00000642914.1:n.934C>T
ENST00000643469.1:c.1951C>T	ENSP00000495070.1:p.Arg651Trp
ENST00000645140.1:c.1863C>T
ENST00000645206.1:n.465C>T
ENST00000645929.1:c.1114C>T	ENSP00000494402.1:p.Arg372Trp
ENST00000646340.1:c.1957C>T	ENSP00000496730.1:p.Arg653Trp
ENST00000646647.2:c.1951C>T MANE Select	ENSP00000495240.1:p.Arg651Trp
ENST00000399982.6:c.1951C>T	ENSP00000382863.2:p.Arg651Trp
ENST00000430710.7:c.1114C>T	ENSP00000406288.3:p.Arg372Trp
ENST00000555962.5:n.151-12549C>T
ENST00000557364.5:c.1951C>T	ENSP00000451601.1:p.Arg651Trp
NM_001170629.1:c.1951C>T	NP_001164100.1:p.Arg651Trp
NM_020920.3:c.1114C>T	NP_065971.2:p.Arg372Trp
NM_001170629.2:c.1951C>T MANE Select	NP_001164100.1:p.Arg651Trp
NM_020920.4:c.1114C>T	NP_065971.2:p.Arg372Trp