Canonical Allele Identifier: CA626780162

Linked Data

dbSNP Id: rs1307645467

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848940_56848957del , CM000679.2:g.56848940_56848957del GRCh38
NC_000017.10:g.54926301_54926318del , CM000679.1:g.54926301_54926318del GRCh37
NC_000017.9:g.52281300_52281317del NCBI36
NG_033888.1:g.19842_19859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+87_1046+104del (DGKE) MANE Select ENSP00000284061.3:n.1046+87_1046+104del
ENST00000648772.1:c.*313+2986_*313+3003del (TRIM25) ENSP00000498158.1:n.*313+2986_*313+3003del
ENST00000284061.7:c.1046+87_1046+104del (DGKE) ENSP00000284061.3:n.1046+87_1046+104del
ENST00000572944.1:c.876+87_876+104del (DGKE)
NM_003647.2:c.1046+87_1046+104del (DGKE) NP_003638.1:n.1046+87_1046+104del
XM_011525394.1:c.1100+87_1100+104del (DGKE) XP_011523696.1:n.1100+87_1100+104del
XM_011525395.1:c.1100+87_1100+104del (DGKE) XP_011523697.1:n.1100+87_1100+104del
XM_011525396.1:c.1100+87_1100+104del (DGKE) XP_011523698.1:n.1100+87_1100+104del
XM_011525397.1:c.1100+87_1100+104del (DGKE) XP_011523699.1:n.1100+87_1100+104del
XM_011525398.1:c.590+87_590+104del (DGKE) XP_011523700.1:n.590+87_590+104del
XR_934581.1:n.1199+87_1199+104del (DGKE)
XM_011525394.3:c.1100+87_1100+104del (DGKE) XP_011523696.1:n.1100+87_1100+104del
XM_011525395.2:c.1100+87_1100+104del (DGKE) XP_011523697.1:n.1100+87_1100+104del
XM_011525396.2:c.1100+87_1100+104del (DGKE) XP_011523698.1:n.1100+87_1100+104del
XM_017025243.2:c.1418+87_1418+104del (DGKE) XP_016880732.1:n.1418+87_1418+104del
XM_017025244.2:c.1100+87_1100+104del (DGKE) XP_016880733.1:n.1100+87_1100+104del
XR_001752670.2:n.1604+87_1604+104del (DGKE)
XR_001752671.1:n.1211+87_1211+104del (DGKE)
XR_001752672.1:n.1212+87_1212+104del (DGKE)
XR_002958079.1:n.1210+87_1210+104del (DGKE)
NM_003647.3:c.1046+87_1046+104del (DGKE) MANE Select NP_003638.1:n.1046+87_1046+104del