Canonical Allele Identifier: CA2532484168

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845552_56845553del , CM000679.2:g.56845552_56845553del GRCh38
NC_000017.10:g.54922913_54922914del , CM000679.1:g.54922913_54922914del GRCh37
NC_000017.9:g.52277912_52277913del NCBI36
NG_033888.1:g.16454_16455del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.625-138_625-137del (DGKE) MANE Select ENSP00000284061.3:n.625-138_625-137del
ENST00000648772.1:c.*314-1762_*314-1761del (TRIM25) ENSP00000498158.1:n.*314-1762_*314-1761del
ENST00000284061.7:c.625-138_625-137del (DGKE) ENSP00000284061.3:n.625-138_625-137del
ENST00000571084.1:n.161-138_161-137del (DGKE)
ENST00000572944.1:c.455-138_455-137del (DGKE)
ENST00000576869.5:n.773-138_773-137del (DGKE)
NM_003647.2:c.625-138_625-137del (DGKE) NP_003638.1:n.625-138_625-137del
XM_011525394.1:c.679-138_679-137del (DGKE) XP_011523696.1:n.679-138_679-137del
XM_011525395.1:c.679-138_679-137del (DGKE) XP_011523697.1:n.679-138_679-137del
XM_011525396.1:c.679-138_679-137del (DGKE) XP_011523698.1:n.679-138_679-137del
XM_011525397.1:c.679-138_679-137del (DGKE) XP_011523699.1:n.679-138_679-137del
XM_011525398.1:c.169-138_169-137del (DGKE) XP_011523700.1:n.169-138_169-137del
XR_934581.1:n.778-138_778-137del (DGKE)
XM_011525394.3:c.679-138_679-137del (DGKE) XP_011523696.1:n.679-138_679-137del
XM_011525395.2:c.679-138_679-137del (DGKE) XP_011523697.1:n.679-138_679-137del
XM_011525396.2:c.679-138_679-137del (DGKE) XP_011523698.1:n.679-138_679-137del
XM_017025243.2:c.625-138_625-137del (DGKE) XP_016880732.1:n.625-138_625-137del
XM_017025244.2:c.679-138_679-137del (DGKE) XP_016880733.1:n.679-138_679-137del
XR_001752670.2:n.811-138_811-137del (DGKE)
XR_001752671.1:n.790-138_790-137del (DGKE)
XR_001752672.1:n.791-138_791-137del (DGKE)
XR_002958079.1:n.789-138_789-137del (DGKE)
NM_003647.3:c.625-138_625-137del (DGKE) MANE Select NP_003638.1:n.625-138_625-137del