Canonical Allele Identifier: CA2122505920
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21393484_21393488delinsTCTTC , CM000676.2:g.21393484_21393488delinsTCTTC GRCh38
NC_000014.8:g.21861643_21861647delinsTCTTC , CM000676.1:g.21861643_21861647delinsTCTTC GRCh37
NC_000014.7:g.20931483_20931487delinsTCTTC NCBI36
NG_021249.1:g.48811_48815delinsGAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.5470_5474delinsGAAGA ENSP00000406288.3:p.Glu1824=
ENST00000555935.2:c.4007_4011delinsGAAGA
ENST00000557364.6:c.6307_6311delinsGAAGA ENSP00000451601.1:p.Glu2103=
ENST00000643469.1:c.6307_6311delinsGAAGA ENSP00000495070.1:p.Glu2103=
ENST00000645206.1:n.5463_5467delinsGAAGA
ENST00000645929.1:c.5470_5474delinsGAAGA ENSP00000494402.1:p.Glu1824=
ENST00000646647.2:c.6307_6311delinsGAAGA MANE Select ENSP00000495240.1:p.Glu2103=
ENST00000399982.6:c.6307_6311delinsGAAGA ENSP00000382863.2:p.Glu2103=
ENST00000430710.7:c.5470_5474delinsGAAGA ENSP00000406288.3:p.Glu1824=
ENST00000557364.5:c.6307_6311delinsGAAGA ENSP00000451601.1:p.Glu2103=
NM_001170629.1:c.6307_6311delinsGAAGA NP_001164100.1:p.Glu2103=
NM_020920.3:c.5470_5474delinsGAAGA NP_065971.2:p.Glu1824=
NM_001170629.2:c.6307_6311delinsGAAGA MANE Select NP_001164100.1:p.Glu2103=
NM_020920.4:c.5470_5474delinsGAAGA NP_065971.2:p.Glu1824=