Canonical Allele Identifier: CA2638886972

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848972_56848975del , CM000679.2:g.56848972_56848975del GRCh38
NC_000017.10:g.54926333_54926336del , CM000679.1:g.54926333_54926336del GRCh37
NC_000017.9:g.52281332_52281335del NCBI36
NG_033888.1:g.19874_19877del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+119_1046+122del (DGKE) MANE Select ENSP00000284061.3:n.1046+119_1046+122del
ENST00000648772.1:c.*313+2968_*313+2971del (TRIM25) ENSP00000498158.1:n.*313+2968_*313+2971del
ENST00000284061.7:c.1046+119_1046+122del (DGKE) ENSP00000284061.3:n.1046+119_1046+122del
ENST00000572944.1:c.876+119_876+122del (DGKE)
NM_003647.2:c.1046+119_1046+122del (DGKE) NP_003638.1:n.1046+119_1046+122del
XM_011525394.1:c.1100+119_1100+122del (DGKE) XP_011523696.1:n.1100+119_1100+122del
XM_011525395.1:c.1100+119_1100+122del (DGKE) XP_011523697.1:n.1100+119_1100+122del
XM_011525396.1:c.1100+119_1100+122del (DGKE) XP_011523698.1:n.1100+119_1100+122del
XM_011525397.1:c.1100+119_1100+122del (DGKE) XP_011523699.1:n.1100+119_1100+122del
XM_011525398.1:c.590+119_590+122del (DGKE) XP_011523700.1:n.590+119_590+122del
XR_934581.1:n.1199+119_1199+122del (DGKE)
XM_011525394.3:c.1100+119_1100+122del (DGKE) XP_011523696.1:n.1100+119_1100+122del
XM_011525395.2:c.1100+119_1100+122del (DGKE) XP_011523697.1:n.1100+119_1100+122del
XM_011525396.2:c.1100+119_1100+122del (DGKE) XP_011523698.1:n.1100+119_1100+122del
XM_017025243.2:c.1418+119_1418+122del (DGKE) XP_016880732.1:n.1418+119_1418+122del
XM_017025244.2:c.1100+119_1100+122del (DGKE) XP_016880733.1:n.1100+119_1100+122del
XR_001752670.2:n.1604+119_1604+122del (DGKE)
XR_001752671.1:n.1211+119_1211+122del (DGKE)
XR_001752672.1:n.1212+119_1212+122del (DGKE)
XR_002958079.1:n.1210+119_1210+122del (DGKE)
NM_003647.3:c.1046+119_1046+122del (DGKE) MANE Select NP_003638.1:n.1046+119_1046+122del