Canonical Allele Identifier: CA2624085017

Gene: CHD8

Linked Data

• dbSNP Id: rs2139498697
• gnomAD v4: 14-21415506-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415508_21415509insTAA , CM000676.2:g.21415508_21415509insTAA	GRCh38
NC_000014.8:g.21883667_21883668insTAA , CM000676.1:g.21883667_21883668insTAA	GRCh37
NC_000014.7:g.20953507_20953508insTAA	NCBI36
NG_021249.1:g.26792_26793insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+67_1131+68insATT	ENSP00000406288.3:n.1131+67_1131+68insATT
ENST00000555962.6:c.-110-12465_-110-12464insATT	ENSP00000495174.1:n.-110-12465_-110-12464insATT
ENST00000557364.6:c.1968+67_1968+68insATT	ENSP00000451601.1:n.1968+67_1968+68insATT
ENST00000642914.1:n.1018_1019insATT
ENST00000643469.1:c.1968+67_1968+68insATT	ENSP00000495070.1:n.1968+67_1968+68insATT
ENST00000645140.1:c.1880+67_1880+68insATT
ENST00000645206.1:n.482+67_482+68insATT
ENST00000645929.1:c.1131+67_1131+68insATT	ENSP00000494402.1:n.1131+67_1131+68insATT
ENST00000646340.1:c.1974+67_1974+68insATT	ENSP00000496730.1:n.1974+67_1974+68insATT
ENST00000646647.2:c.1968+67_1968+68insATT MANE Select	ENSP00000495240.1:n.1968+67_1968+68insATT
ENST00000399982.6:c.1968+67_1968+68insATT	ENSP00000382863.2:n.1968+67_1968+68insATT
ENST00000430710.7:c.1131+67_1131+68insATT	ENSP00000406288.3:n.1131+67_1131+68insATT
ENST00000555962.5:n.151-12465_151-12464insATT
ENST00000557364.5:c.1968+67_1968+68insATT	ENSP00000451601.1:n.1968+67_1968+68insATT
NM_001170629.1:c.1968+67_1968+68insATT	NP_001164100.1:n.1968+67_1968+68insATT
NM_020920.3:c.1131+67_1131+68insATT	NP_065971.2:n.1131+67_1131+68insATT
NM_001170629.2:c.1968+67_1968+68insATT MANE Select	NP_001164100.1:n.1968+67_1968+68insATT
NM_020920.4:c.1131+67_1131+68insATT	NP_065971.2:n.1131+67_1131+68insATT