Canonical Allele Identifier: CA2122502268
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21405716C= , CM000676.2:g.21405716C= GRCh38
NC_000014.8:g.21873875C= , CM000676.1:g.21873875C= GRCh37
NC_000014.7:g.20943715C= NCBI36
NG_021249.1:g.36583G=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.2214+5G= ENSP00000406288.3:n.2214+5G=
ENST00000555935.2:c.727+5G=
ENST00000555962.6:c.-110-2674G= ENSP00000495174.1:n.-110-2674G=
ENST00000557364.6:c.3051+5G= ENSP00000451601.1:n.3051+5G=
ENST00000643469.1:c.3051+5G= ENSP00000495070.1:n.3051+5G=
ENST00000645140.1:c.2963+5G=
ENST00000645206.1:n.1565+5G=
ENST00000645929.1:c.2214+5G= ENSP00000494402.1:n.2214+5G=
ENST00000646340.1:c.3057+5G= ENSP00000496730.1:n.3057+5G=
ENST00000646647.2:c.3051+5G= MANE Select ENSP00000495240.1:n.3051+5G=
ENST00000399982.6:c.3051+5G= ENSP00000382863.2:n.3051+5G=
ENST00000430710.7:c.2214+5G= ENSP00000406288.3:n.2214+5G=
ENST00000555935.1:c.727+5G=
ENST00000555962.5:n.151-2674G=
ENST00000557364.5:c.3051+5G= ENSP00000451601.1:n.3051+5G=
NM_001170629.1:c.3051+5G= NP_001164100.1:n.3051+5G=
NM_020920.3:c.2214+5G= NP_065971.2:n.2214+5G=
NM_001170629.2:c.3051+5G= MANE Select NP_001164100.1:n.3051+5G=
NM_020920.4:c.2214+5G= NP_065971.2:n.2214+5G=