Canonical Allele Identifier: CA341649526

Gene: DDX20

Linked Data

• MyVariant Identifiers: chr1:g.112309136A>T (hg19) ; chr1:g.111766514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111766514A>T , CM000663.2:g.111766514A>T	GRCh38
NC_000001.10:g.112309136A>T , CM000663.1:g.112309136A>T	GRCh37
NC_000001.9:g.112110659A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369702.5:c.2090A>T MANE Select	ENSP00000358716.4:p.Glu697Val
ENST00000533164.6:c.*1504A>T	ENSP00000434085.1:n.*1504A>T
ENST00000534200.2:n.3825A>T
ENST00000679381.1:n.2712A>T
ENST00000679498.1:n.3948A>T
ENST00000679576.1:c.2425A>T	ENSP00000506357.1:n.2425A>T
ENST00000679724.1:c.2090A>T	ENSP00000505857.1:p.Glu697Val
ENST00000679774.1:n.3715A>T
ENST00000680038.1:n.3082A>T
ENST00000680317.1:n.2438A>T
ENST00000680383.1:c.*969A>T	ENSP00000505119.1:n.*969A>T
ENST00000680415.1:n.3421A>T
ENST00000680518.1:c.*816A>T	ENSP00000506543.1:n.*816A>T
ENST00000680627.1:c.2090A>T	ENSP00000505758.1:p.Glu697Val
ENST00000680936.1:c.*1318A>T	ENSP00000506651.1:n.*1318A>T
ENST00000680983.1:n.1959A>T
ENST00000681529.1:n.2812A>T
ENST00000681559.1:c.*1267A>T	ENSP00000506100.1:n.*1267A>T
ENST00000681747.1:n.3090A>T
ENST00000369702.4:c.2090A>T	ENSP00000358716.4:p.Glu697Val
ENST00000475700.1:c.914A>T	ENSP00000435660.1:p.Glu305Val
NM_007204.4:c.2090A>T	NP_009135.4:p.Glu697Val
NM_007204.5:c.2090A>T MANE Select	NP_009135.4:p.Glu697Val