Canonical Allele Identifier: CA2122483230
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21409895C= , CM000676.2:g.21409895C= GRCh38
NC_000014.8:g.21878054C= , CM000676.1:g.21878054C= GRCh37
NC_000014.7:g.20947894C= NCBI36
NG_021249.1:g.32404G=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.1483G= ENSP00000406288.3:p.Glu495=
ENST00000555962.6:c.-110-6853G= ENSP00000495174.1:n.-110-6853G=
ENST00000557364.6:c.2320G= ENSP00000451601.1:p.Glu774=
ENST00000643469.1:c.2320G= ENSP00000495070.1:p.Glu774=
ENST00000645140.1:c.2232G=
ENST00000645206.1:n.834G=
ENST00000645929.1:c.1483G= ENSP00000494402.1:p.Glu495=
ENST00000646340.1:c.2326G= ENSP00000496730.1:p.Glu776=
ENST00000646647.2:c.2320G= MANE Select ENSP00000495240.1:p.Glu774=
ENST00000399982.6:c.2320G= ENSP00000382863.2:p.Glu774=
ENST00000430710.7:c.1483G= ENSP00000406288.3:p.Glu495=
ENST00000554384.1:n.188G=
ENST00000555962.5:n.151-6853G=
ENST00000557364.5:c.2320G= ENSP00000451601.1:p.Glu774=
NM_001170629.1:c.2320G= NP_001164100.1:p.Glu774=
NM_020920.3:c.1483G= NP_065971.2:p.Glu495=
NM_001170629.2:c.2320G= MANE Select NP_001164100.1:p.Glu774=
NM_020920.4:c.1483G= NP_065971.2:p.Glu495=