Canonical Allele Identifier: CA1189057879
Gene: DDX20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111766502G= , CM000663.2:g.111766502G= GRCh38
NC_000001.10:g.112309124G= , CM000663.1:g.112309124G= GRCh37
NC_000001.9:g.112110647G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369702.5:c.2078G= MANE Select ENSP00000358716.4:p.Arg693=
ENST00000533164.6:c.*1492G= ENSP00000434085.1:n.*1492G=
ENST00000534200.2:n.3813G=
ENST00000679381.1:n.2700G=
ENST00000679498.1:n.3936G=
ENST00000679576.1:c.2413G= ENSP00000506357.1:n.2413G=
ENST00000679724.1:c.2078G= ENSP00000505857.1:p.Arg693=
ENST00000679774.1:n.3703G=
ENST00000680038.1:n.3070G=
ENST00000680317.1:n.2426G=
ENST00000680383.1:c.*957G= ENSP00000505119.1:n.*957G=
ENST00000680415.1:n.3409G=
ENST00000680518.1:c.*804G= ENSP00000506543.1:n.*804G=
ENST00000680627.1:c.2078G= ENSP00000505758.1:p.Arg693=
ENST00000680936.1:c.*1306G= ENSP00000506651.1:n.*1306G=
ENST00000680983.1:n.1947G=
ENST00000681529.1:n.2800G=
ENST00000681559.1:c.*1255G= ENSP00000506100.1:n.*1255G=
ENST00000681747.1:n.3078G=
ENST00000369702.4:c.2078G= ENSP00000358716.4:p.Arg693=
ENST00000475700.1:c.902G= ENSP00000435660.1:p.Arg301=
NM_007204.4:c.2078G= NP_009135.4:p.Arg693=
NM_007204.5:c.2078G= MANE Select NP_009135.4:p.Arg693=