Canonical Allele Identifier: CA2122505063
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21428152A= , CM000676.2:g.21428152A= GRCh38
NC_000014.8:g.21896311A= , CM000676.1:g.21896311A= GRCh37
NC_000014.7:g.20966151A= NCBI36
NG_021249.1:g.14147T=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.481T= ENSP00000406288.3:p.Ser161=
ENST00000553651.2:n.3124T=
ENST00000555962.6:c.-111+3659T= ENSP00000495174.1:n.-111+3659T=
ENST00000557364.6:c.1318T= ENSP00000451601.1:p.Ser440=
ENST00000642518.1:c.481T= ENSP00000496722.1:p.Ser161=
ENST00000643048.1:n.1613T=
ENST00000643469.1:c.1318T= ENSP00000495070.1:p.Ser440=
ENST00000645140.1:c.1230T=
ENST00000645929.1:c.481T= ENSP00000494402.1:p.Ser161=
ENST00000646063.1:c.1405T= ENSP00000496565.1:p.Ser469=
ENST00000646340.1:c.1324T= ENSP00000496730.1:p.Ser442=
ENST00000646647.2:c.1318T= MANE Select ENSP00000495240.1:p.Ser440=
ENST00000399982.6:c.1318T= ENSP00000382863.2:p.Ser440=
ENST00000430710.7:c.481T= ENSP00000406288.3:p.Ser161=
ENST00000555962.5:n.150+3659T=
ENST00000557364.5:c.1318T= ENSP00000451601.1:p.Ser440=
NM_001170629.1:c.1318T= NP_001164100.1:p.Ser440=
NM_020920.3:c.481T= NP_065971.2:p.Ser161=
NM_001170629.2:c.1318T= MANE Select NP_001164100.1:p.Ser440=
NM_020920.4:c.481T= NP_065971.2:p.Ser161=