Canonical Allele Identifier: CA2266993640

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845663_56845664delinsCT , CM000679.2:g.56845663_56845664delinsCT	GRCh38
NC_000017.10:g.54923024_54923025delinsCT , CM000679.1:g.54923024_54923025delinsCT	GRCh37
NC_000017.9:g.52278023_52278024delinsCT	NCBI36
NG_033888.1:g.16565_16566delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.625-27_625-26delinsCT (DGKE) MANE Select	ENSP00000284061.3:n.625-27_625-26delinsCT
ENST00000648772.1:c.*314-1874_*314-1873delinsAG (TRIM25)	ENSP00000498158.1:n.*314-1874_*314-1873delinsAG
ENST00000284061.7:c.625-27_625-26delinsCT (DGKE)	ENSP00000284061.3:n.625-27_625-26delinsCT
ENST00000571084.1:n.161-27_161-26delinsCT (DGKE)
ENST00000572944.1:c.455-27_455-26delinsCT (DGKE)
ENST00000576869.5:n.773-27_773-26delinsCT (DGKE)
NM_003647.2:c.625-27_625-26delinsCT (DGKE)	NP_003638.1:n.625-27_625-26delinsCT
XM_011525394.1:c.679-27_679-26delinsCT (DGKE)	XP_011523696.1:n.679-27_679-26delinsCT
XM_011525395.1:c.679-27_679-26delinsCT (DGKE)	XP_011523697.1:n.679-27_679-26delinsCT
XM_011525396.1:c.679-27_679-26delinsCT (DGKE)	XP_011523698.1:n.679-27_679-26delinsCT
XM_011525397.1:c.679-27_679-26delinsCT (DGKE)	XP_011523699.1:n.679-27_679-26delinsCT
XM_011525398.1:c.169-27_169-26delinsCT (DGKE)	XP_011523700.1:n.169-27_169-26delinsCT
XR_934581.1:n.778-27_778-26delinsCT (DGKE)
XM_011525394.3:c.679-27_679-26delinsCT (DGKE)	XP_011523696.1:n.679-27_679-26delinsCT
XM_011525395.2:c.679-27_679-26delinsCT (DGKE)	XP_011523697.1:n.679-27_679-26delinsCT
XM_011525396.2:c.679-27_679-26delinsCT (DGKE)	XP_011523698.1:n.679-27_679-26delinsCT
XM_017025243.2:c.625-27_625-26delinsCT (DGKE)	XP_016880732.1:n.625-27_625-26delinsCT
XM_017025244.2:c.679-27_679-26delinsCT (DGKE)	XP_016880733.1:n.679-27_679-26delinsCT
XR_001752670.2:n.811-27_811-26delinsCT (DGKE)
XR_001752671.1:n.790-27_790-26delinsCT (DGKE)
XR_001752672.1:n.791-27_791-26delinsCT (DGKE)
XR_002958079.1:n.789-27_789-26delinsCT (DGKE)
NM_003647.3:c.625-27_625-26delinsCT (DGKE) MANE Select	NP_003638.1:n.625-27_625-26delinsCT