Canonical Allele Identifier: CA2838301623
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21393697dup , CM000676.2:g.21393697dup GRCh38
NC_000014.8:g.21861856dup , CM000676.1:g.21861856dup GRCh37
NC_000014.7:g.20931696dup NCBI36
NG_021249.1:g.48603dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.5262dup ENSP00000406288.3:p.Ser1755GlufsTer9
ENST00000555935.2:c.3799dup
ENST00000557364.6:c.6099dup ENSP00000451601.1:p.Ser2034GlufsTer9
ENST00000643469.1:c.6099dup ENSP00000495070.1:p.Ser2034GlufsTer9
ENST00000645206.1:n.5255dup
ENST00000645929.1:c.5262dup ENSP00000494402.1:p.Ser1755GlufsTer9
ENST00000646647.2:c.6099dup MANE Select ENSP00000495240.1:p.Ser2034GlufsTer9
ENST00000399982.6:c.6099dup ENSP00000382863.2:p.Ser2034GlufsTer9
ENST00000430710.7:c.5262dup ENSP00000406288.3:p.Ser1755GlufsTer9
ENST00000555301.1:n.893dup
ENST00000557364.5:c.6099dup ENSP00000451601.1:p.Ser2034GlufsTer9
NM_001170629.1:c.6099dup NP_001164100.1:p.Ser2034GlufsTer9
NM_020920.3:c.5262dup NP_065971.2:p.Ser1755GlufsTer9
NM_001170629.2:c.6099dup MANE Select NP_001164100.1:p.Ser2034GlufsTer9
NM_020920.4:c.5262dup NP_065971.2:p.Ser1755GlufsTer9