Canonical Allele Identifier: CA500687349

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1191749965
• gnomAD v3: 17-56848779-A-G
• gnomAD v4: 17-56848779-A-G
• MyVariant Identifiers: chr17:g.54926140A>G (hg19) ; chr17:g.56848779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848779A>G , CM000679.2:g.56848779A>G	GRCh38
NC_000017.10:g.54926140A>G , CM000679.1:g.54926140A>G	GRCh37
NC_000017.9:g.52281139A>G	NCBI36
NG_033888.1:g.19681A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.972A>G (DGKE) MANE Select	ENSP00000284061.3:p.Thr324=
ENST00000648772.1:c.*313+3164T>C (TRIM25)	ENSP00000498158.1:n.*313+3164T>C
ENST00000284061.7:c.972A>G (DGKE)	ENSP00000284061.3:p.Thr324=
ENST00000572944.1:c.802A>G (DGKE)
NM_003647.2:c.972A>G (DGKE)	NP_003638.1:p.Thr324=
XM_011525394.1:c.1026A>G (DGKE)	XP_011523696.1:p.Thr342=
XM_011525395.1:c.1026A>G (DGKE)	XP_011523697.1:p.Thr342=
XM_011525396.1:c.1026A>G (DGKE)	XP_011523698.1:p.Thr342=
XM_011525397.1:c.1026A>G (DGKE)	XP_011523699.1:p.Thr342=
XM_011525398.1:c.516A>G (DGKE)	XP_011523700.1:p.Thr172=
XR_934581.1:n.1125A>G (DGKE)
XM_011525394.3:c.1026A>G (DGKE)	XP_011523696.1:p.Thr342=
XM_011525395.2:c.1026A>G (DGKE)	XP_011523697.1:p.Thr342=
XM_011525396.2:c.1026A>G (DGKE)	XP_011523698.1:p.Thr342=
XM_017025243.2:c.1344A>G (DGKE)	XP_016880732.1:p.Thr448=
XM_017025244.2:c.1026A>G (DGKE)	XP_016880733.1:p.Thr342=
XR_001752670.2:n.1530A>G (DGKE)
XR_001752671.1:n.1137A>G (DGKE)
XR_001752672.1:n.1138A>G (DGKE)
XR_002958079.1:n.1136A>G (DGKE)
NM_003647.3:c.972A>G (DGKE) MANE Select	NP_003638.1:p.Thr324=