Canonical Allele Identifier: CA2624082356

Gene: CHD8

Linked Data

• dbSNP Id: rs2139484491
• gnomAD v4: 14-21409771-AAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21409777_21409779del , CM000676.2:g.21409777_21409779del	GRCh38
NC_000014.8:g.21877936_21877938del , CM000676.1:g.21877936_21877938del	GRCh37
NC_000014.7:g.20947776_20947778del	NCBI36
NG_021249.1:g.32525_32527del

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.1527+77_1527+79del	ENSP00000406288.3:n.1527+77_1527+79del
ENST00000555935.2:c.40+77_40+79del
ENST00000555962.6:c.-110-6732_-110-6730del	ENSP00000495174.1:n.-110-6732_-110-6730de...
ENST00000557364.6:c.2364+77_2364+79del	ENSP00000451601.1:n.2364+77_2364+79del
ENST00000643469.1:c.2364+77_2364+79del	ENSP00000495070.1:n.2364+77_2364+79del
ENST00000645140.1:c.2276+77_2276+79del
ENST00000645206.1:n.878+77_878+79del
ENST00000645929.1:c.1527+77_1527+79del	ENSP00000494402.1:n.1527+77_1527+79del
ENST00000646340.1:c.2370+77_2370+79del	ENSP00000496730.1:n.2370+77_2370+79del
ENST00000646647.2:c.2364+77_2364+79del MANE Select	ENSP00000495240.1:n.2364+77_2364+79del
ENST00000399982.6:c.2364+77_2364+79del	ENSP00000382863.2:n.2364+77_2364+79del
ENST00000430710.7:c.1527+77_1527+79del	ENSP00000406288.3:n.1527+77_1527+79del
ENST00000554384.1:n.232+77_232+79del
ENST00000555935.1:c.40+77_40+79del
ENST00000555962.5:n.151-6732_151-6730del
ENST00000557364.5:c.2364+77_2364+79del	ENSP00000451601.1:n.2364+77_2364+79del
NM_001170629.1:c.2364+77_2364+79del	NP_001164100.1:n.2364+77_2364+79del
NM_020920.3:c.1527+77_1527+79del	NP_065971.2:n.1527+77_1527+79del
NM_001170629.2:c.2364+77_2364+79del MANE Select	NP_001164100.1:n.2364+77_2364+79del
NM_020920.4:c.1527+77_1527+79del	NP_065971.2:n.1527+77_1527+79del