Canonical Allele Identifier: CA2575477601

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415545_21415546insTAAAT , CM000676.2:g.21415545_21415546insTAAAT	GRCh38
NC_000014.8:g.21883704_21883705insTAAAT , CM000676.1:g.21883704_21883705insTAAAT	GRCh37
NC_000014.7:g.20953544_20953545insTAAAT	NCBI36
NG_021249.1:g.26753_26754insATTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+28_1131+29insATTTA	ENSP00000406288.3:n.1131+28_1131+29insATTTA
ENST00000555962.6:c.-110-12504_-110-12503insATTTA	ENSP00000495174.1:n.-110-12504_-110-12503insATTTA
ENST00000557364.6:c.1968+28_1968+29insATTTA	ENSP00000451601.1:n.1968+28_1968+29insATTTA
ENST00000642914.1:n.979_980insATTTA
ENST00000643469.1:c.1968+28_1968+29insATTTA	ENSP00000495070.1:n.1968+28_1968+29insATTTA
ENST00000645140.1:c.1880+28_1880+29insATTTA
ENST00000645206.1:n.482+28_482+29insATTTA
ENST00000645929.1:c.1131+28_1131+29insATTTA	ENSP00000494402.1:n.1131+28_1131+29insATTTA
ENST00000646340.1:c.1974+28_1974+29insATTTA	ENSP00000496730.1:n.1974+28_1974+29insATTTA
ENST00000646647.2:c.1968+28_1968+29insATTTA MANE Select	ENSP00000495240.1:n.1968+28_1968+29insATTTA
ENST00000399982.6:c.1968+28_1968+29insATTTA	ENSP00000382863.2:n.1968+28_1968+29insATTTA
ENST00000430710.7:c.1131+28_1131+29insATTTA	ENSP00000406288.3:n.1131+28_1131+29insATTTA
ENST00000555962.5:n.151-12504_151-12503insATTTA
ENST00000557364.5:c.1968+28_1968+29insATTTA	ENSP00000451601.1:n.1968+28_1968+29insATTTA
NM_001170629.1:c.1968+28_1968+29insATTTA	NP_001164100.1:n.1968+28_1968+29insATTTA
NM_020920.3:c.1131+28_1131+29insATTTA	NP_065971.2:n.1131+28_1131+29insATTTA
NM_001170629.2:c.1968+28_1968+29insATTTA MANE Select	NP_001164100.1:n.1968+28_1968+29insATTTA
NM_020920.4:c.1131+28_1131+29insATTTA	NP_065971.2:n.1131+28_1131+29insATTTA