Canonical Allele Identifier: CA388876373
Gene: CHD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21409854C>A , CM000676.2:g.21409854C>A GRCh38
NC_000014.8:g.21878013C>A , CM000676.1:g.21878013C>A GRCh37
NC_000014.7:g.20947853C>A NCBI36
NG_021249.1:g.32445G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.1524G>T ENSP00000406288.3:p.Arg508Ser
ENST00000555935.2:c.37G>T
ENST00000555962.6:c.-110-6812G>T ENSP00000495174.1:n.-110-6812G>T
ENST00000557364.6:c.2361G>T ENSP00000451601.1:p.Arg787Ser
ENST00000643469.1:c.2361G>T ENSP00000495070.1:p.Arg787Ser
ENST00000645140.1:c.2273G>T
ENST00000645206.1:n.875G>T
ENST00000645929.1:c.1524G>T ENSP00000494402.1:p.Arg508Ser
ENST00000646340.1:c.2367G>T ENSP00000496730.1:p.Arg789Ser
ENST00000646647.2:c.2361G>T MANE Select ENSP00000495240.1:p.Arg787Ser
ENST00000399982.6:c.2361G>T ENSP00000382863.2:p.Arg787Ser
ENST00000430710.7:c.1524G>T ENSP00000406288.3:p.Arg508Ser
ENST00000554384.1:n.229G>T
ENST00000555935.1:c.37G>T
ENST00000555962.5:n.151-6812G>T
ENST00000557364.5:c.2361G>T ENSP00000451601.1:p.Arg787Ser
NM_001170629.1:c.2361G>T NP_001164100.1:p.Arg787Ser
NM_020920.3:c.1524G>T NP_065971.2:p.Arg508Ser
NM_001170629.2:c.2361G>T MANE Select NP_001164100.1:p.Arg787Ser
NM_020920.4:c.1524G>T NP_065971.2:p.Arg508Ser