Canonical Allele Identifier: CA645590768

Gene: CHD8

Linked Data

• COSMIC: COSM3737169 ; COSM3737170

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21409843_21409846del , CM000676.2:g.21409843_21409846del	GRCh38
NC_000014.8:g.21878002_21878005del , CM000676.1:g.21878002_21878005del	GRCh37
NC_000014.7:g.20947842_20947845del	NCBI36
NG_021249.1:g.32453_32456del

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.1527+5_1527+8del	ENSP00000406288.3:n.1527+5_1527+8del
ENST00000555935.2:c.40+5_40+8del
ENST00000555962.6:c.-110-6804_-110-6801del	ENSP00000495174.1:n.-110-6804_-110-6801de...
ENST00000557364.6:c.2364+5_2364+8del	ENSP00000451601.1:n.2364+5_2364+8del
ENST00000643469.1:c.2364+5_2364+8del	ENSP00000495070.1:n.2364+5_2364+8del
ENST00000645140.1:c.2276+5_2276+8del
ENST00000645206.1:n.878+5_878+8del
ENST00000645929.1:c.1527+5_1527+8del	ENSP00000494402.1:n.1527+5_1527+8del
ENST00000646340.1:c.2370+5_2370+8del	ENSP00000496730.1:n.2370+5_2370+8del
ENST00000646647.2:c.2364+5_2364+8del MANE Select	ENSP00000495240.1:n.2364+5_2364+8del
ENST00000399982.6:c.2364+5_2364+8del	ENSP00000382863.2:n.2364+5_2364+8del
ENST00000430710.7:c.1527+5_1527+8del	ENSP00000406288.3:n.1527+5_1527+8del
ENST00000554384.1:n.232+5_232+8del
ENST00000555935.1:c.40+5_40+8del
ENST00000555962.5:n.151-6804_151-6801del
ENST00000557364.5:c.2364+5_2364+8del	ENSP00000451601.1:n.2364+5_2364+8del
NM_001170629.1:c.2364+5_2364+8del	NP_001164100.1:n.2364+5_2364+8del
NM_020920.3:c.1527+5_1527+8del	NP_065971.2:n.1527+5_1527+8del
NM_001170629.2:c.2364+5_2364+8del MANE Select	NP_001164100.1:n.2364+5_2364+8del
NM_020920.4:c.1527+5_1527+8del	NP_065971.2:n.1527+5_1527+8del