Canonical Allele Identifier: CA8663577

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs754556879
• ExAC: 17:54923121 T / C
• gnomAD v2: 17-54923121-T-C
• gnomAD v3: 17-56845760-T-C
• gnomAD v4: 17-56845760-T-C
• MyVariant Identifiers: chr17:g.54923121T>C (hg19) ; chr17:g.56845760T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845760T>C , CM000679.2:g.56845760T>C	GRCh38
NC_000017.10:g.54923121T>C , CM000679.1:g.54923121T>C	GRCh37
NC_000017.9:g.52278120T>C	NCBI36
NG_033888.1:g.16662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.695T>C (DGKE) MANE Select	ENSP00000284061.3:p.Met232Thr
ENST00000648772.1:c.*314-1970A>G (TRIM25)	ENSP00000498158.1:n.*314-1970A>G
ENST00000284061.7:c.695T>C (DGKE)	ENSP00000284061.3:p.Met232Thr
ENST00000571084.1:n.231T>C (DGKE)
ENST00000572944.1:c.525T>C (DGKE)
ENST00000576869.5:n.843T>C (DGKE)
NM_003647.2:c.695T>C (DGKE)	NP_003638.1:p.Met232Thr
XM_011525394.1:c.749T>C (DGKE)	XP_011523696.1:p.Met250Thr
XM_011525395.1:c.749T>C (DGKE)	XP_011523697.1:p.Met250Thr
XM_011525396.1:c.749T>C (DGKE)	XP_011523698.1:p.Met250Thr
XM_011525397.1:c.749T>C (DGKE)	XP_011523699.1:p.Met250Thr
XM_011525398.1:c.239T>C (DGKE)	XP_011523700.1:p.Met80Thr
XR_934581.1:n.848T>C (DGKE)
XM_011525394.3:c.749T>C (DGKE)	XP_011523696.1:p.Met250Thr
XM_011525395.2:c.749T>C (DGKE)	XP_011523697.1:p.Met250Thr
XM_011525396.2:c.749T>C (DGKE)	XP_011523698.1:p.Met250Thr
XM_017025243.2:c.695T>C (DGKE)	XP_016880732.1:p.Met232Thr
XM_017025244.2:c.749T>C (DGKE)	XP_016880733.1:p.Met250Thr
XR_001752670.2:n.881T>C (DGKE)
XR_001752671.1:n.860T>C (DGKE)
XR_001752672.1:n.861T>C (DGKE)
XR_002958079.1:n.859T>C (DGKE)
NM_003647.3:c.695T>C (DGKE) MANE Select	NP_003638.1:p.Met232Thr