Canonical Allele Identifier: CA645571677

Gene: CHD8

Linked Data

• COSMIC: COSM4445234 ; COSM4445235

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21393567del , CM000676.2:g.21393567del	GRCh38
NC_000014.8:g.21861726del , CM000676.1:g.21861726del	GRCh37
NC_000014.7:g.20931566del	NCBI36
NG_021249.1:g.48732del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.5391del	ENSP00000406288.3:p.Ser1797ArgfsTer?
ENST00000555935.2:c.3928del
ENST00000557364.6:c.6228del	ENSP00000451601.1:p.Ser2076ArgfsTer?
ENST00000643469.1:c.6228del	ENSP00000495070.1:p.Ser2076ArgfsTer?
ENST00000645206.1:n.5384del
ENST00000645929.1:c.5391del	ENSP00000494402.1:p.Ser1797ArgfsTer?
ENST00000646647.2:c.6228del MANE Select	ENSP00000495240.1:p.Ser2076ArgfsTer?
ENST00000399982.6:c.6228del	ENSP00000382863.2:p.Ser2076ArgfsTer?
ENST00000430710.7:c.5391del	ENSP00000406288.3:p.Ser1797ArgfsTer?
ENST00000557364.5:c.6228del	ENSP00000451601.1:p.Ser2076ArgfsTer?
NM_001170629.1:c.6228del	NP_001164100.1:p.Ser2076ArgfsTer?
NM_020920.3:c.5391del	NP_065971.2:p.Ser1797ArgfsTer?
NM_001170629.2:c.6228del MANE Select	NP_001164100.1:p.Ser2076ArgfsTer?
NM_020920.4:c.5391del	NP_065971.2:p.Ser1797ArgfsTer?