Canonical Allele Identifier: CA1142435924
Gene: DDX20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111766509T= , CM000663.2:g.111766509T= GRCh38
NC_000001.10:g.112309131T= , CM000663.1:g.112309131T= GRCh37
NC_000001.9:g.112110654T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369702.5:c.2085T= MANE Select ENSP00000358716.4:p.Ser695=
ENST00000533164.6:c.*1499T= ENSP00000434085.1:n.*1499T=
ENST00000534200.2:n.3820T=
ENST00000679381.1:n.2707T=
ENST00000679498.1:n.3943T=
ENST00000679576.1:c.2420T= ENSP00000506357.1:n.2420T=
ENST00000679724.1:c.2085T= ENSP00000505857.1:p.Ser695=
ENST00000679774.1:n.3710T=
ENST00000680038.1:n.3077T=
ENST00000680317.1:n.2433T=
ENST00000680383.1:c.*964T= ENSP00000505119.1:n.*964T=
ENST00000680415.1:n.3416T=
ENST00000680518.1:c.*811T= ENSP00000506543.1:n.*811T=
ENST00000680627.1:c.2085T= ENSP00000505758.1:p.Ser695=
ENST00000680936.1:c.*1313T= ENSP00000506651.1:n.*1313T=
ENST00000680983.1:n.1954T=
ENST00000681529.1:n.2807T=
ENST00000681559.1:c.*1262T= ENSP00000506100.1:n.*1262T=
ENST00000681747.1:n.3085T=
ENST00000369702.4:c.2085T= ENSP00000358716.4:p.Ser695=
ENST00000475700.1:c.909T= ENSP00000435660.1:p.Ser303=
NM_007204.4:c.2085T= NP_009135.4:p.Ser695=
NM_007204.5:c.2085T= MANE Select NP_009135.4:p.Ser695=