Canonical Allele Identifier: CA2122502394
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21405789C= , CM000676.2:g.21405789C= GRCh38
NC_000014.8:g.21873948C= , CM000676.1:g.21873948C= GRCh37
NC_000014.7:g.20943788C= NCBI36
NG_021249.1:g.36510G=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.2146G= ENSP00000406288.3:p.Glu716=
ENST00000555935.2:c.659G=
ENST00000555962.6:c.-110-2747G= ENSP00000495174.1:n.-110-2747G=
ENST00000557364.6:c.2983G= ENSP00000451601.1:p.Glu995=
ENST00000643469.1:c.2983G= ENSP00000495070.1:p.Glu995=
ENST00000645140.1:c.2895G=
ENST00000645206.1:n.1497G=
ENST00000645929.1:c.2146G= ENSP00000494402.1:p.Glu716=
ENST00000646340.1:c.2989G= ENSP00000496730.1:p.Glu997=
ENST00000646647.2:c.2983G= MANE Select ENSP00000495240.1:p.Glu995=
ENST00000399982.6:c.2983G= ENSP00000382863.2:p.Glu995=
ENST00000430710.7:c.2146G= ENSP00000406288.3:p.Glu716=
ENST00000555935.1:c.659G=
ENST00000555962.5:n.151-2747G=
ENST00000557364.5:c.2983G= ENSP00000451601.1:p.Glu995=
NM_001170629.1:c.2983G= NP_001164100.1:p.Glu995=
NM_020920.3:c.2146G= NP_065971.2:p.Glu716=
NM_001170629.2:c.2983G= MANE Select NP_001164100.1:p.Glu995=
NM_020920.4:c.2146G= NP_065971.2:p.Glu716=