Canonical Allele Identifier: CA388883864
Gene: CHD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21394930C>G , CM000676.2:g.21394930C>G GRCh38
NC_000014.8:g.21863089C>G , CM000676.1:g.21863089C>G GRCh37
NC_000014.7:g.20932929C>G NCBI36
NG_021249.1:g.47369G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.4535G>C ENSP00000406288.3:p.Arg1512Pro
ENST00000555935.2:c.3072G>C
ENST00000555962.6:c.*757G>C ENSP00000495174.1:n.*757G>C
ENST00000557364.6:c.5372G>C ENSP00000451601.1:p.Arg1791Pro
ENST00000643469.1:c.5372G>C ENSP00000495070.1:p.Arg1791Pro
ENST00000645206.1:n.4528G>C
ENST00000645929.1:c.4535G>C ENSP00000494402.1:p.Arg1512Pro
ENST00000646340.1:c.5378G>C ENSP00000496730.1:p.Arg1793Pro
ENST00000646647.2:c.5372G>C MANE Select ENSP00000495240.1:p.Arg1791Pro
ENST00000399982.6:c.5372G>C ENSP00000382863.2:p.Arg1791Pro
ENST00000430710.7:c.4535G>C ENSP00000406288.3:p.Arg1512Pro
ENST00000555301.1:n.85G>C
ENST00000557364.5:c.5372G>C ENSP00000451601.1:p.Arg1791Pro
NM_001170629.1:c.5372G>C NP_001164100.1:p.Arg1791Pro
NM_020920.3:c.4535G>C NP_065971.2:p.Arg1512Pro
NM_001170629.2:c.5372G>C MANE Select NP_001164100.1:p.Arg1791Pro
NM_020920.4:c.4535G>C NP_065971.2:p.Arg1512Pro