Canonical Allele Identifier: CA291904504

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs867685255
• gnomAD v2: 17-54921418-T-C
• gnomAD v4: 17-56844057-T-C
• MyVariant Identifiers: chr17:g.54921418T>C (hg19) ; chr17:g.56844057T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56844057T>C , CM000679.2:g.56844057T>C	GRCh38
NC_000017.10:g.54921418T>C , CM000679.1:g.54921418T>C	GRCh37
NC_000017.9:g.52276417T>C	NCBI36
NG_033888.1:g.14959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.503T>C (DGKE) MANE Select	ENSP00000284061.3:p.Met168Thr
ENST00000648772.1:c.*314-267A>G (TRIM25)	ENSP00000498158.1:n.*314-267A>G
ENST00000284061.7:c.503T>C (DGKE)	ENSP00000284061.3:p.Met168Thr
ENST00000571084.1:n.39T>C (DGKE)
ENST00000572944.1:c.333T>C (DGKE)
ENST00000576869.5:n.651T>C (DGKE)
NM_003647.2:c.503T>C (DGKE)	NP_003638.1:p.Met168Thr
XM_011525394.1:c.557T>C (DGKE)	XP_011523696.1:p.Met186Thr
XM_011525395.1:c.557T>C (DGKE)	XP_011523697.1:p.Met186Thr
XM_011525396.1:c.557T>C (DGKE)	XP_011523698.1:p.Met186Thr
XM_011525397.1:c.557T>C (DGKE)	XP_011523699.1:p.Met186Thr
XM_011525398.1:c.47T>C (DGKE)	XP_011523700.1:p.Met16Thr
XR_934581.1:n.656T>C (DGKE)
XM_011525394.3:c.557T>C (DGKE)	XP_011523696.1:p.Met186Thr
XM_011525395.2:c.557T>C (DGKE)	XP_011523697.1:p.Met186Thr
XM_011525396.2:c.557T>C (DGKE)	XP_011523698.1:p.Met186Thr
XM_017025243.2:c.503T>C (DGKE)	XP_016880732.1:p.Met168Thr
XM_017025244.2:c.557T>C (DGKE)	XP_016880733.1:p.Met186Thr
XR_001752670.2:n.689T>C (DGKE)
XR_001752671.1:n.668T>C (DGKE)
XR_001752672.1:n.669T>C (DGKE)
XR_002958079.1:n.667T>C (DGKE)
NM_003647.3:c.503T>C (DGKE) MANE Select	NP_003638.1:p.Met168Thr