Canonical Allele Identifier: CA2266995220

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56849004_56849008delinsTTATG , CM000679.2:g.56849004_56849008delinsTTATG	GRCh38
NC_000017.10:g.54926365_54926369delinsTTATG , CM000679.1:g.54926365_54926369delinsTTATG	GRCh37
NC_000017.9:g.52281364_52281368delinsTTATG	NCBI36
NG_033888.1:g.19906_19910delinsTTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+151_1046+155delinsTTATG (DGKE) MANE Select	ENSP00000284061.3:n.1046+151_1046+155delinsTTATG
ENST00000648772.1:c.*313+2935_*313+2939delinsCATAA (TRIM25)	ENSP00000498158.1:n.*313+2935_*313+2939delinsCATAA
ENST00000284061.7:c.1046+151_1046+155delinsTTATG (DGKE)	ENSP00000284061.3:n.1046+151_1046+155delinsTTATG
ENST00000572944.1:c.876+151_876+155delinsTTATG (DGKE)
NM_003647.2:c.1046+151_1046+155delinsTTATG (DGKE)	NP_003638.1:n.1046+151_1046+155delinsTTATG
XM_011525394.1:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523696.1:n.1100+151_1100+155delinsTTATG
XM_011525395.1:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523697.1:n.1100+151_1100+155delinsTTATG
XM_011525396.1:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523698.1:n.1100+151_1100+155delinsTTATG
XM_011525397.1:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523699.1:n.1100+151_1100+155delinsTTATG
XM_011525398.1:c.590+151_590+155delinsTTATG (DGKE)	XP_011523700.1:n.590+151_590+155delinsTTATG
XR_934581.1:n.1199+151_1199+155delinsTTATG (DGKE)
XM_011525394.3:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523696.1:n.1100+151_1100+155delinsTTATG
XM_011525395.2:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523697.1:n.1100+151_1100+155delinsTTATG
XM_011525396.2:c.1100+151_1100+155delinsTTATG (DGKE)	XP_011523698.1:n.1100+151_1100+155delinsTTATG
XM_017025243.2:c.1418+151_1418+155delinsTTATG (DGKE)	XP_016880732.1:n.1418+151_1418+155delinsTTATG
XM_017025244.2:c.1100+151_1100+155delinsTTATG (DGKE)	XP_016880733.1:n.1100+151_1100+155delinsTTATG
XR_001752670.2:n.1604+151_1604+155delinsTTATG (DGKE)
XR_001752671.1:n.1211+151_1211+155delinsTTATG (DGKE)
XR_001752672.1:n.1212+151_1212+155delinsTTATG (DGKE)
XR_002958079.1:n.1210+151_1210+155delinsTTATG (DGKE)
NM_003647.3:c.1046+151_1046+155delinsTTATG (DGKE) MANE Select	NP_003638.1:n.1046+151_1046+155delinsTTATG