Canonical Allele Identifier: CA2122489239

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415544_21415548delinsAAAAT , CM000676.2:g.21415544_21415548delinsAAAAT	GRCh38
NC_000014.8:g.21883703_21883707delinsAAAAT , CM000676.1:g.21883703_21883707delinsAAAAT	GRCh37
NC_000014.7:g.20953543_20953547delinsAAAAT	NCBI36
NG_021249.1:g.26751_26755delinsATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+26_1131+30delinsATTTT	ENSP00000406288.3:n.1131+26_1131+30delinsATTTT
ENST00000555962.6:c.-110-12506_-110-12502delinsATTTT	ENSP00000495174.1:n.-110-12506_-110-12502delinsATTTT
ENST00000557364.6:c.1968+26_1968+30delinsATTTT	ENSP00000451601.1:n.1968+26_1968+30delinsATTTT
ENST00000642914.1:n.977_981delinsATTTT
ENST00000643469.1:c.1968+26_1968+30delinsATTTT	ENSP00000495070.1:n.1968+26_1968+30delinsATTTT
ENST00000645140.1:c.1880+26_1880+30delinsATTTT
ENST00000645206.1:n.482+26_482+30delinsATTTT
ENST00000645929.1:c.1131+26_1131+30delinsATTTT	ENSP00000494402.1:n.1131+26_1131+30delinsATTTT
ENST00000646340.1:c.1974+26_1974+30delinsATTTT	ENSP00000496730.1:n.1974+26_1974+30delinsATTTT
ENST00000646647.2:c.1968+26_1968+30delinsATTTT MANE Select	ENSP00000495240.1:n.1968+26_1968+30delinsATTTT
ENST00000399982.6:c.1968+26_1968+30delinsATTTT	ENSP00000382863.2:n.1968+26_1968+30delinsATTTT
ENST00000430710.7:c.1131+26_1131+30delinsATTTT	ENSP00000406288.3:n.1131+26_1131+30delinsATTTT
ENST00000555962.5:n.151-12506_151-12502delinsATTTT
ENST00000557364.5:c.1968+26_1968+30delinsATTTT	ENSP00000451601.1:n.1968+26_1968+30delinsATTTT
NM_001170629.1:c.1968+26_1968+30delinsATTTT	NP_001164100.1:n.1968+26_1968+30delinsATTTT
NM_020920.3:c.1131+26_1131+30delinsATTTT	NP_065971.2:n.1131+26_1131+30delinsATTTT
NM_001170629.2:c.1968+26_1968+30delinsATTTT MANE Select	NP_001164100.1:n.1968+26_1968+30delinsATTTT
NM_020920.4:c.1131+26_1131+30delinsATTTT	NP_065971.2:n.1131+26_1131+30delinsATTTT