Canonical Allele Identifier: CA2122489847
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21415880G= , CM000676.2:g.21415880G= GRCh38
NC_000014.8:g.21884039G= , CM000676.1:g.21884039G= GRCh37
NC_000014.7:g.20953879G= NCBI36
NG_021249.1:g.26419C=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.907C= ENSP00000406288.3:p.Arg303=
ENST00000555962.6:c.-110-12838C= ENSP00000495174.1:n.-110-12838C=
ENST00000557364.6:c.1744C= ENSP00000451601.1:p.Arg582=
ENST00000642518.1:c.907C= ENSP00000496722.1:p.Arg303=
ENST00000642914.1:n.727C=
ENST00000643469.1:c.1744C= ENSP00000495070.1:p.Arg582=
ENST00000645140.1:c.1656C=
ENST00000645206.1:n.258C=
ENST00000645929.1:c.907C= ENSP00000494402.1:p.Arg303=
ENST00000646340.1:c.1750C= ENSP00000496730.1:p.Arg584=
ENST00000646647.2:c.1744C= MANE Select ENSP00000495240.1:p.Arg582=
ENST00000399982.6:c.1744C= ENSP00000382863.2:p.Arg582=
ENST00000430710.7:c.907C= ENSP00000406288.3:p.Arg303=
ENST00000555962.5:n.151-12838C=
ENST00000557364.5:c.1744C= ENSP00000451601.1:p.Arg582=
NM_001170629.1:c.1744C= NP_001164100.1:p.Arg582=
NM_020920.3:c.907C= NP_065971.2:p.Arg303=
NM_001170629.2:c.1744C= MANE Select NP_001164100.1:p.Arg582=
NM_020920.4:c.907C= NP_065971.2:p.Arg303=