Canonical Allele Identifier: CA2122506244
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21429317T= , CM000676.2:g.21429317T= GRCh38
NC_000014.8:g.21897476T= , CM000676.1:g.21897476T= GRCh37
NC_000014.7:g.20967316T= NCBI36
NG_021249.1:g.12982A=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.25A= ENSP00000406288.3:p.Thr9=
ENST00000553651.2:n.2668A=
ENST00000555962.6:c.-111+2494A= ENSP00000495174.1:n.-111+2494A=
ENST00000557364.6:c.862A= ENSP00000451601.1:p.Thr288=
ENST00000642518.1:c.25A= ENSP00000496722.1:p.Thr9=
ENST00000643048.1:n.1157A=
ENST00000643469.1:c.862A= ENSP00000495070.1:p.Thr288=
ENST00000645140.1:c.774A=
ENST00000645929.1:c.25A= ENSP00000494402.1:p.Thr9=
ENST00000646063.1:c.949A= ENSP00000496565.1:p.Thr317=
ENST00000646340.1:c.868A= ENSP00000496730.1:p.Thr290=
ENST00000646647.2:c.862A= MANE Select ENSP00000495240.1:p.Thr288=
ENST00000399982.6:c.862A= ENSP00000382863.2:p.Thr288=
ENST00000430710.7:c.25A= ENSP00000406288.3:p.Thr9=
ENST00000553283.1:c.115A= ENSP00000450860.1:p.Thr39=
ENST00000555962.5:n.150+2494A=
ENST00000557364.5:c.862A= ENSP00000451601.1:p.Thr288=
NM_001170629.1:c.862A= NP_001164100.1:p.Thr288=
NM_020920.3:c.25A= NP_065971.2:p.Thr9=
NM_001170629.2:c.862A= MANE Select NP_001164100.1:p.Thr288=
NM_020920.4:c.25A= NP_065971.2:p.Thr9=