Canonical Allele Identifier: CA2576328918

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845713_56845722del , CM000679.2:g.56845713_56845722del GRCh38
NC_000017.10:g.54923074_54923083del , CM000679.1:g.54923074_54923083del GRCh37
NC_000017.9:g.52278073_52278082del NCBI36
NG_033888.1:g.16615_16624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.648_657del (DGKE) MANE Select ENSP00000284061.3:p.Gln216HisfsTer2
ENST00000648772.1:c.*314-1930_*314-1921del (TRIM25) ENSP00000498158.1:n.*314-1930_*314-1921del
ENST00000284061.7:c.648_657del (DGKE) ENSP00000284061.3:p.Gln216HisfsTer2
ENST00000571084.1:n.184_193del (DGKE)
ENST00000572944.1:c.478_487del (DGKE)
ENST00000576869.5:n.796_805del (DGKE)
NM_003647.2:c.648_657del (DGKE) NP_003638.1:p.Gln216HisfsTer2
XM_011525394.1:c.702_711del (DGKE) XP_011523696.1:p.Gln234HisfsTer2
XM_011525395.1:c.702_711del (DGKE) XP_011523697.1:p.Gln234HisfsTer2
XM_011525396.1:c.702_711del (DGKE) XP_011523698.1:p.Gln234HisfsTer2
XM_011525397.1:c.702_711del (DGKE) XP_011523699.1:p.Gln234HisfsTer2
XM_011525398.1:c.192_201del (DGKE) XP_011523700.1:p.Gln64HisfsTer2
XR_934581.1:n.801_810del (DGKE)
XM_011525394.3:c.702_711del (DGKE) XP_011523696.1:p.Gln234HisfsTer2
XM_011525395.2:c.702_711del (DGKE) XP_011523697.1:p.Gln234HisfsTer2
XM_011525396.2:c.702_711del (DGKE) XP_011523698.1:p.Gln234HisfsTer2
XM_017025243.2:c.648_657del (DGKE) XP_016880732.1:p.Gln216HisfsTer2
XM_017025244.2:c.702_711del (DGKE) XP_016880733.1:p.Gln234HisfsTer2
XR_001752670.2:n.834_843del (DGKE)
XR_001752671.1:n.813_822del (DGKE)
XR_001752672.1:n.814_823del (DGKE)
XR_002958079.1:n.812_821del (DGKE)
NM_003647.3:c.648_657del (DGKE) MANE Select NP_003638.1:p.Gln216HisfsTer2