Canonical Allele Identifier: CA2122495176
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21401080A= , CM000676.2:g.21401080A= GRCh38
NC_000014.8:g.21869239A= , CM000676.1:g.21869239A= GRCh37
NC_000014.7:g.20939079A= NCBI36
NG_021249.1:g.41219T=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.3337-9T= ENSP00000406288.3:n.3337-9T=
ENST00000555935.2:c.1850-9T=
ENST00000555962.6:c.265-773T= ENSP00000495174.1:n.265-773T=
ENST00000557364.6:c.4174-9T= ENSP00000451601.1:n.4174-9T=
ENST00000643469.1:c.4174-9T= ENSP00000495070.1:n.4174-9T=
ENST00000645206.1:n.2688-9T=
ENST00000645929.1:c.3337-9T= ENSP00000494402.1:n.3337-9T=
ENST00000646340.1:c.4180-9T= ENSP00000496730.1:n.4180-9T=
ENST00000646558.1:n.728-9T=
ENST00000646647.2:c.4174-9T= MANE Select ENSP00000495240.1:n.4174-9T=
ENST00000399982.6:c.4174-9T= ENSP00000382863.2:n.4174-9T=
ENST00000430710.7:c.3337-9T= ENSP00000406288.3:n.3337-9T=
ENST00000555935.1:c.1850-9T=
ENST00000555962.5:n.525-773T=
ENST00000557364.5:c.4174-9T= ENSP00000451601.1:n.4174-9T=
NM_001170629.1:c.4174-9T= NP_001164100.1:n.4174-9T=
NM_020920.3:c.3337-9T= NP_065971.2:n.3337-9T=
NM_001170629.2:c.4174-9T= MANE Select NP_001164100.1:n.4174-9T=
NM_020920.4:c.3337-9T= NP_065971.2:n.3337-9T=