Canonical Allele Identifier: CA1189057881
Gene: DDX20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111766511T= , CM000663.2:g.111766511T= GRCh38
NC_000001.10:g.112309133T= , CM000663.1:g.112309133T= GRCh37
NC_000001.9:g.112110656T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369702.5:c.2087T= MANE Select ENSP00000358716.4:p.Leu696=
ENST00000533164.6:c.*1501T= ENSP00000434085.1:n.*1501T=
ENST00000534200.2:n.3822T=
ENST00000679381.1:n.2709T=
ENST00000679498.1:n.3945T=
ENST00000679576.1:c.2422T= ENSP00000506357.1:n.2422T=
ENST00000679724.1:c.2087T= ENSP00000505857.1:p.Leu696=
ENST00000679774.1:n.3712T=
ENST00000680038.1:n.3079T=
ENST00000680317.1:n.2435T=
ENST00000680383.1:c.*966T= ENSP00000505119.1:n.*966T=
ENST00000680415.1:n.3418T=
ENST00000680518.1:c.*813T= ENSP00000506543.1:n.*813T=
ENST00000680627.1:c.2087T= ENSP00000505758.1:p.Leu696=
ENST00000680936.1:c.*1315T= ENSP00000506651.1:n.*1315T=
ENST00000680983.1:n.1956T=
ENST00000681529.1:n.2809T=
ENST00000681559.1:c.*1264T= ENSP00000506100.1:n.*1264T=
ENST00000681747.1:n.3087T=
ENST00000369702.4:c.2087T= ENSP00000358716.4:p.Leu696=
ENST00000475700.1:c.911T= ENSP00000435660.1:p.Leu304=
NM_007204.4:c.2087T= NP_009135.4:p.Leu696=
NM_007204.5:c.2087T= MANE Select NP_009135.4:p.Leu696=