Canonical Allele Identifier: CA2122505040
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21428148C= , CM000676.2:g.21428148C= GRCh38
NC_000014.8:g.21896307C= , CM000676.1:g.21896307C= GRCh37
NC_000014.7:g.20966147C= NCBI36
NG_021249.1:g.14151G=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.485G= ENSP00000406288.3:p.Gly162=
ENST00000553651.2:n.3128G=
ENST00000555962.6:c.-111+3663G= ENSP00000495174.1:n.-111+3663G=
ENST00000557364.6:c.1322G= ENSP00000451601.1:p.Gly441=
ENST00000642518.1:c.485G= ENSP00000496722.1:p.Gly162=
ENST00000643048.1:n.1617G=
ENST00000643469.1:c.1322G= ENSP00000495070.1:p.Gly441=
ENST00000645140.1:c.1234G=
ENST00000645929.1:c.485G= ENSP00000494402.1:p.Gly162=
ENST00000646063.1:c.1409G= ENSP00000496565.1:p.Gly470=
ENST00000646340.1:c.1328G= ENSP00000496730.1:p.Gly443=
ENST00000646647.2:c.1322G= MANE Select ENSP00000495240.1:p.Gly441=
ENST00000399982.6:c.1322G= ENSP00000382863.2:p.Gly441=
ENST00000430710.7:c.485G= ENSP00000406288.3:p.Gly162=
ENST00000555962.5:n.150+3663G=
ENST00000557364.5:c.1322G= ENSP00000451601.1:p.Gly441=
NM_001170629.1:c.1322G= NP_001164100.1:p.Gly441=
NM_020920.3:c.485G= NP_065971.2:p.Gly162=
NM_001170629.2:c.1322G= MANE Select NP_001164100.1:p.Gly441=
NM_020920.4:c.485G= NP_065971.2:p.Gly162=