Canonical Allele Identifier: CA399928000

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1268143568
• gnomAD v2: 17-54926183-G-A
• gnomAD v3: 17-56848822-G-A
• gnomAD v4: 17-56848822-G-A
• MyVariant Identifiers: chr17:g.54926183G>A (hg19) ; chr17:g.56848822G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848822G>A , CM000679.2:g.56848822G>A	GRCh38
NC_000017.10:g.54926183G>A , CM000679.1:g.54926183G>A	GRCh37
NC_000017.9:g.52281182G>A	NCBI36
NG_033888.1:g.19724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1015G>A (DGKE) MANE Select	ENSP00000284061.3:p.Val339Ile
ENST00000648772.1:c.*313+3121C>T (TRIM25)	ENSP00000498158.1:n.*313+3121C>T
ENST00000284061.7:c.1015G>A (DGKE)	ENSP00000284061.3:p.Val339Ile
ENST00000572944.1:c.845G>A (DGKE)
NM_003647.2:c.1015G>A (DGKE)	NP_003638.1:p.Val339Ile
XM_011525394.1:c.1069G>A (DGKE)	XP_011523696.1:p.Val357Ile
XM_011525395.1:c.1069G>A (DGKE)	XP_011523697.1:p.Val357Ile
XM_011525396.1:c.1069G>A (DGKE)	XP_011523698.1:p.Val357Ile
XM_011525397.1:c.1069G>A (DGKE)	XP_011523699.1:p.Val357Ile
XM_011525398.1:c.559G>A (DGKE)	XP_011523700.1:p.Val187Ile
XR_934581.1:n.1168G>A (DGKE)
XM_011525394.3:c.1069G>A (DGKE)	XP_011523696.1:p.Val357Ile
XM_011525395.2:c.1069G>A (DGKE)	XP_011523697.1:p.Val357Ile
XM_011525396.2:c.1069G>A (DGKE)	XP_011523698.1:p.Val357Ile
XM_017025243.2:c.1387G>A (DGKE)	XP_016880732.1:p.Val463Ile
XM_017025244.2:c.1069G>A (DGKE)	XP_016880733.1:p.Val357Ile
XR_001752670.2:n.1573G>A (DGKE)
XR_001752671.1:n.1180G>A (DGKE)
XR_001752672.1:n.1181G>A (DGKE)
XR_002958079.1:n.1179G>A (DGKE)
NM_003647.3:c.1015G>A (DGKE) MANE Select	NP_003638.1:p.Val339Ile