Canonical Allele Identifier: CA2595898821

Gene: DGKE TRIM25

Linked Data

• gnomAD v3: 17-56848937-T-TGGTC
• gnomAD v4: 17-56848937-T-TGGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848938_56848939insGTCG , CM000679.2:g.56848938_56848939insGTCG	GRCh38
NC_000017.10:g.54926299_54926300insGTCG , CM000679.1:g.54926299_54926300insGTCG	GRCh37
NC_000017.9:g.52281298_52281299insGTCG	NCBI36
NG_033888.1:g.19840_19841insGTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+85_1046+86insGTCG (DGKE) MANE Select	ENSP00000284061.3:n.1046+85_1046+86insGTCG
ENST00000648772.1:c.*313+3005_*313+3006insGACC (TRIM25)	ENSP00000498158.1:n.*313+3005_*313+3006insGACC
ENST00000284061.7:c.1046+85_1046+86insGTCG (DGKE)	ENSP00000284061.3:n.1046+85_1046+86insGTCG
ENST00000572944.1:c.876+85_876+86insGTCG (DGKE)
NM_003647.2:c.1046+85_1046+86insGTCG (DGKE)	NP_003638.1:n.1046+85_1046+86insGTCG
XM_011525394.1:c.1100+85_1100+86insGTCG (DGKE)	XP_011523696.1:n.1100+85_1100+86insGTCG
XM_011525395.1:c.1100+85_1100+86insGTCG (DGKE)	XP_011523697.1:n.1100+85_1100+86insGTCG
XM_011525396.1:c.1100+85_1100+86insGTCG (DGKE)	XP_011523698.1:n.1100+85_1100+86insGTCG
XM_011525397.1:c.1100+85_1100+86insGTCG (DGKE)	XP_011523699.1:n.1100+85_1100+86insGTCG
XM_011525398.1:c.590+85_590+86insGTCG (DGKE)	XP_011523700.1:n.590+85_590+86insGTCG
XR_934581.1:n.1199+85_1199+86insGTCG (DGKE)
XM_011525394.3:c.1100+85_1100+86insGTCG (DGKE)	XP_011523696.1:n.1100+85_1100+86insGTCG
XM_011525395.2:c.1100+85_1100+86insGTCG (DGKE)	XP_011523697.1:n.1100+85_1100+86insGTCG
XM_011525396.2:c.1100+85_1100+86insGTCG (DGKE)	XP_011523698.1:n.1100+85_1100+86insGTCG
XM_017025243.2:c.1418+85_1418+86insGTCG (DGKE)	XP_016880732.1:n.1418+85_1418+86insGTCG
XM_017025244.2:c.1100+85_1100+86insGTCG (DGKE)	XP_016880733.1:n.1100+85_1100+86insGTCG
XR_001752670.2:n.1604+85_1604+86insGTCG (DGKE)
XR_001752671.1:n.1211+85_1211+86insGTCG (DGKE)
XR_001752672.1:n.1212+85_1212+86insGTCG (DGKE)
XR_002958079.1:n.1210+85_1210+86insGTCG (DGKE)
NM_003647.3:c.1046+85_1046+86insGTCG (DGKE) MANE Select	NP_003638.1:n.1046+85_1046+86insGTCG