Canonical Allele Identifier: CA1139778285
Gene: DDX20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111766501C= , CM000663.2:g.111766501C= GRCh38
NC_000001.10:g.112309123C= , CM000663.1:g.112309123C= GRCh37
NC_000001.9:g.112110646C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369702.5:c.2077C= MANE Select ENSP00000358716.4:p.Arg693=
ENST00000533164.6:c.*1491C= ENSP00000434085.1:n.*1491C=
ENST00000534200.2:n.3812C=
ENST00000679381.1:n.2699C=
ENST00000679498.1:n.3935C=
ENST00000679576.1:c.2412C= ENSP00000506357.1:n.2412C=
ENST00000679724.1:c.2077C= ENSP00000505857.1:p.Arg693=
ENST00000679774.1:n.3702C=
ENST00000680038.1:n.3069C=
ENST00000680317.1:n.2425C=
ENST00000680383.1:c.*956C= ENSP00000505119.1:n.*956C=
ENST00000680415.1:n.3408C=
ENST00000680518.1:c.*803C= ENSP00000506543.1:n.*803C=
ENST00000680627.1:c.2077C= ENSP00000505758.1:p.Arg693=
ENST00000680936.1:c.*1305C= ENSP00000506651.1:n.*1305C=
ENST00000680983.1:n.1946C=
ENST00000681529.1:n.2799C=
ENST00000681559.1:c.*1254C= ENSP00000506100.1:n.*1254C=
ENST00000681747.1:n.3077C=
ENST00000369702.4:c.2077C= ENSP00000358716.4:p.Arg693=
ENST00000475700.1:c.901C= ENSP00000435660.1:p.Arg301=
NM_007204.4:c.2077C= NP_009135.4:p.Arg693=
NM_007204.5:c.2077C= MANE Select NP_009135.4:p.Arg693=