Canonical Allele Identifier: CA626783510

Linked Data

dbSNP Id: rs1489259170

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56849007_56849010del , CM000679.2:g.56849007_56849010del GRCh38
NC_000017.10:g.54926368_54926371del , CM000679.1:g.54926368_54926371del GRCh37
NC_000017.9:g.52281367_52281370del NCBI36
NG_033888.1:g.19909_19912del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+154_1046+157del (DGKE) MANE Select ENSP00000284061.3:n.1046+154_1046+157del
ENST00000648772.1:c.*313+2935_*313+2938del (TRIM25) ENSP00000498158.1:n.*313+2935_*313+2938del
ENST00000284061.7:c.1046+154_1046+157del (DGKE) ENSP00000284061.3:n.1046+154_1046+157del
ENST00000572944.1:c.876+154_876+157del (DGKE)
NM_003647.2:c.1046+154_1046+157del (DGKE) NP_003638.1:n.1046+154_1046+157del
XM_011525394.1:c.1100+154_1100+157del (DGKE) XP_011523696.1:n.1100+154_1100+157del
XM_011525395.1:c.1100+154_1100+157del (DGKE) XP_011523697.1:n.1100+154_1100+157del
XM_011525396.1:c.1100+154_1100+157del (DGKE) XP_011523698.1:n.1100+154_1100+157del
XM_011525397.1:c.1100+154_1100+157del (DGKE) XP_011523699.1:n.1100+154_1100+157del
XM_011525398.1:c.590+154_590+157del (DGKE) XP_011523700.1:n.590+154_590+157del
XR_934581.1:n.1199+154_1199+157del (DGKE)
XM_011525394.3:c.1100+154_1100+157del (DGKE) XP_011523696.1:n.1100+154_1100+157del
XM_011525395.2:c.1100+154_1100+157del (DGKE) XP_011523697.1:n.1100+154_1100+157del
XM_011525396.2:c.1100+154_1100+157del (DGKE) XP_011523698.1:n.1100+154_1100+157del
XM_017025243.2:c.1418+154_1418+157del (DGKE) XP_016880732.1:n.1418+154_1418+157del
XM_017025244.2:c.1100+154_1100+157del (DGKE) XP_016880733.1:n.1100+154_1100+157del
XR_001752670.2:n.1604+154_1604+157del (DGKE)
XR_001752671.1:n.1211+154_1211+157del (DGKE)
XR_001752672.1:n.1212+154_1212+157del (DGKE)
XR_002958079.1:n.1210+154_1210+157del (DGKE)
NM_003647.3:c.1046+154_1046+157del (DGKE) MANE Select NP_003638.1:n.1046+154_1046+157del