Canonical Allele Identifier: CA419696419

Gene: DDX20

Linked Data

• MyVariant Identifiers: chr1:g.112309128T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111766506T>C , CM000663.2:g.111766506T>C	GRCh38
NC_000001.10:g.112309128T>C , CM000663.1:g.112309128T>C	GRCh37
NC_000001.9:g.112110651T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369702.5:c.2082T>C MANE Select	ENSP00000358716.4:p.Ile694=
ENST00000533164.6:c.*1496T>C	ENSP00000434085.1:n.*1496T>C
ENST00000534200.2:n.3817T>C
ENST00000679381.1:n.2704T>C
ENST00000679498.1:n.3940T>C
ENST00000679576.1:c.2417T>C	ENSP00000506357.1:n.2417T>C
ENST00000679724.1:c.2082T>C	ENSP00000505857.1:p.Ile694=
ENST00000679774.1:n.3707T>C
ENST00000680038.1:n.3074T>C
ENST00000680317.1:n.2430T>C
ENST00000680383.1:c.*961T>C	ENSP00000505119.1:n.*961T>C
ENST00000680415.1:n.3413T>C
ENST00000680518.1:c.*808T>C	ENSP00000506543.1:n.*808T>C
ENST00000680627.1:c.2082T>C	ENSP00000505758.1:p.Ile694=
ENST00000680936.1:c.*1310T>C	ENSP00000506651.1:n.*1310T>C
ENST00000680983.1:n.1951T>C
ENST00000681529.1:n.2804T>C
ENST00000681559.1:c.*1259T>C	ENSP00000506100.1:n.*1259T>C
ENST00000681747.1:n.3082T>C
ENST00000369702.4:c.2082T>C	ENSP00000358716.4:p.Ile694=
ENST00000475700.1:c.906T>C	ENSP00000435660.1:p.Ile302=
NM_007204.4:c.2082T>C	NP_009135.4:p.Ile694=
NM_007204.5:c.2082T>C MANE Select	NP_009135.4:p.Ile694=