Canonical Allele Identifier: CA2122489141

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415537_21415538delinsAT , CM000676.2:g.21415537_21415538delinsAT	GRCh38
NC_000014.8:g.21883696_21883697delinsAT , CM000676.1:g.21883696_21883697delinsAT	GRCh37
NC_000014.7:g.20953536_20953537delinsAT	NCBI36
NG_021249.1:g.26761_26762delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+36_1131+37delinsAT	ENSP00000406288.3:n.1131+36_1131+37delinsAT
ENST00000555962.6:c.-110-12496_-110-12495delinsAT	ENSP00000495174.1:n.-110-12496_-110-12495delinsAT
ENST00000557364.6:c.1968+36_1968+37delinsAT	ENSP00000451601.1:n.1968+36_1968+37delinsAT
ENST00000642914.1:n.987_988delinsAT
ENST00000643469.1:c.1968+36_1968+37delinsAT	ENSP00000495070.1:n.1968+36_1968+37delinsAT
ENST00000645140.1:c.1880+36_1880+37delinsAT
ENST00000645206.1:n.482+36_482+37delinsAT
ENST00000645929.1:c.1131+36_1131+37delinsAT	ENSP00000494402.1:n.1131+36_1131+37delinsAT
ENST00000646340.1:c.1974+36_1974+37delinsAT	ENSP00000496730.1:n.1974+36_1974+37delinsAT
ENST00000646647.2:c.1968+36_1968+37delinsAT MANE Select	ENSP00000495240.1:n.1968+36_1968+37delinsAT
ENST00000399982.6:c.1968+36_1968+37delinsAT	ENSP00000382863.2:n.1968+36_1968+37delinsAT
ENST00000430710.7:c.1131+36_1131+37delinsAT	ENSP00000406288.3:n.1131+36_1131+37delinsAT
ENST00000555962.5:n.151-12496_151-12495delinsAT
ENST00000557364.5:c.1968+36_1968+37delinsAT	ENSP00000451601.1:n.1968+36_1968+37delinsAT
NM_001170629.1:c.1968+36_1968+37delinsAT	NP_001164100.1:n.1968+36_1968+37delinsAT
NM_020920.3:c.1131+36_1131+37delinsAT	NP_065971.2:n.1131+36_1131+37delinsAT
NM_001170629.2:c.1968+36_1968+37delinsAT MANE Select	NP_001164100.1:n.1968+36_1968+37delinsAT
NM_020920.4:c.1131+36_1131+37delinsAT	NP_065971.2:n.1131+36_1131+37delinsAT