Canonical Allele Identifier: CA2638886965

Gene: DGKE TRIM25

Linked Data

• gnomAD v4: 17-56848964-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848964_56848965insG , CM000679.2:g.56848964_56848965insG	GRCh38
NC_000017.10:g.54926325_54926326insG , CM000679.1:g.54926325_54926326insG	GRCh37
NC_000017.9:g.52281324_52281325insG	NCBI36
NG_033888.1:g.19866_19867insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+111_1046+112insG (DGKE) MANE Select	ENSP00000284061.3:n.1046+111_1046+112insG
ENST00000648772.1:c.*313+2978_*313+2979insC (TRIM25)	ENSP00000498158.1:n.*313+2978_*313+2979insC
ENST00000284061.7:c.1046+111_1046+112insG (DGKE)	ENSP00000284061.3:n.1046+111_1046+112insG
ENST00000572944.1:c.876+111_876+112insG (DGKE)
NM_003647.2:c.1046+111_1046+112insG (DGKE)	NP_003638.1:n.1046+111_1046+112insG
XM_011525394.1:c.1100+111_1100+112insG (DGKE)	XP_011523696.1:n.1100+111_1100+112insG
XM_011525395.1:c.1100+111_1100+112insG (DGKE)	XP_011523697.1:n.1100+111_1100+112insG
XM_011525396.1:c.1100+111_1100+112insG (DGKE)	XP_011523698.1:n.1100+111_1100+112insG
XM_011525397.1:c.1100+111_1100+112insG (DGKE)	XP_011523699.1:n.1100+111_1100+112insG
XM_011525398.1:c.590+111_590+112insG (DGKE)	XP_011523700.1:n.590+111_590+112insG
XR_934581.1:n.1199+111_1199+112insG (DGKE)
XM_011525394.3:c.1100+111_1100+112insG (DGKE)	XP_011523696.1:n.1100+111_1100+112insG
XM_011525395.2:c.1100+111_1100+112insG (DGKE)	XP_011523697.1:n.1100+111_1100+112insG
XM_011525396.2:c.1100+111_1100+112insG (DGKE)	XP_011523698.1:n.1100+111_1100+112insG
XM_017025243.2:c.1418+111_1418+112insG (DGKE)	XP_016880732.1:n.1418+111_1418+112insG
XM_017025244.2:c.1100+111_1100+112insG (DGKE)	XP_016880733.1:n.1100+111_1100+112insG
XR_001752670.2:n.1604+111_1604+112insG (DGKE)
XR_001752671.1:n.1211+111_1211+112insG (DGKE)
XR_001752672.1:n.1212+111_1212+112insG (DGKE)
XR_002958079.1:n.1210+111_1210+112insG (DGKE)
NM_003647.3:c.1046+111_1046+112insG (DGKE) MANE Select	NP_003638.1:n.1046+111_1046+112insG