Canonical Allele Identifier: CA341649495

Gene: DDX20

Linked Data

• MyVariant Identifiers: chr1:g.112309129T>A (hg19) ; chr1:g.111766507T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111766507T>A , CM000663.2:g.111766507T>A	GRCh38
NC_000001.10:g.112309129T>A , CM000663.1:g.112309129T>A	GRCh37
NC_000001.9:g.112110652T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369702.5:c.2083T>A MANE Select	ENSP00000358716.4:p.Ser695Thr
ENST00000533164.6:c.*1497T>A	ENSP00000434085.1:n.*1497T>A
ENST00000534200.2:n.3818T>A
ENST00000679381.1:n.2705T>A
ENST00000679498.1:n.3941T>A
ENST00000679576.1:c.2418T>A	ENSP00000506357.1:n.2418T>A
ENST00000679724.1:c.2083T>A	ENSP00000505857.1:p.Ser695Thr
ENST00000679774.1:n.3708T>A
ENST00000680038.1:n.3075T>A
ENST00000680317.1:n.2431T>A
ENST00000680383.1:c.*962T>A	ENSP00000505119.1:n.*962T>A
ENST00000680415.1:n.3414T>A
ENST00000680518.1:c.*809T>A	ENSP00000506543.1:n.*809T>A
ENST00000680627.1:c.2083T>A	ENSP00000505758.1:p.Ser695Thr
ENST00000680936.1:c.*1311T>A	ENSP00000506651.1:n.*1311T>A
ENST00000680983.1:n.1952T>A
ENST00000681529.1:n.2805T>A
ENST00000681559.1:c.*1260T>A	ENSP00000506100.1:n.*1260T>A
ENST00000681747.1:n.3083T>A
ENST00000369702.4:c.2083T>A	ENSP00000358716.4:p.Ser695Thr
ENST00000475700.1:c.907T>A	ENSP00000435660.1:p.Ser303Thr
NM_007204.4:c.2083T>A	NP_009135.4:p.Ser695Thr
NM_007204.5:c.2083T>A MANE Select	NP_009135.4:p.Ser695Thr