Canonical Allele Identifier: CA2266995011

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848514_56848515delinsGC , CM000679.2:g.56848514_56848515delinsGC GRCh38
NC_000017.10:g.54925875_54925876delinsGC , CM000679.1:g.54925875_54925876delinsGC GRCh37
NC_000017.9:g.52280874_52280875delinsGC NCBI36
NG_033888.1:g.19416_19417delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.889-182_889-181delinsGC (DGKE) MANE Select ENSP00000284061.3:n.889-182_889-181delins...
ENST00000648772.1:c.*313+3428_*313+3429delinsGC (TRIM25) ENSP00000498158.1:n.*313+3428_*313+3429de...
ENST00000284061.7:c.889-182_889-181delinsGC (DGKE) ENSP00000284061.3:n.889-182_889-181delins...
ENST00000572944.1:c.719-182_719-181delinsGC (DGKE)
NM_003647.2:c.889-182_889-181delinsGC (DGKE) NP_003638.1:n.889-182_889-181delinsGC
XM_011525394.1:c.943-182_943-181delinsGC (DGKE) XP_011523696.1:n.943-182_943-181delinsGC
XM_011525395.1:c.943-182_943-181delinsGC (DGKE) XP_011523697.1:n.943-182_943-181delinsGC
XM_011525396.1:c.943-182_943-181delinsGC (DGKE) XP_011523698.1:n.943-182_943-181delinsGC
XM_011525397.1:c.943-182_943-181delinsGC (DGKE) XP_011523699.1:n.943-182_943-181delinsGC
XM_011525398.1:c.433-182_433-181delinsGC (DGKE) XP_011523700.1:n.433-182_433-181delinsGC
XR_934581.1:n.1042-182_1042-181delinsGC (DGKE)
XM_011525394.3:c.943-182_943-181delinsGC (DGKE) XP_011523696.1:n.943-182_943-181delinsGC
XM_011525395.2:c.943-182_943-181delinsGC (DGKE) XP_011523697.1:n.943-182_943-181delinsGC
XM_011525396.2:c.943-182_943-181delinsGC (DGKE) XP_011523698.1:n.943-182_943-181delinsGC
XM_017025243.2:c.1260+77_1260+78delinsGC (DGKE) XP_016880732.1:n.1260+77_1260+78delinsGC
XM_017025244.2:c.943-182_943-181delinsGC (DGKE) XP_016880733.1:n.943-182_943-181delinsGC
XR_001752670.2:n.1446+77_1446+78delinsGC (DGKE)
XR_001752671.1:n.1054-182_1054-181delinsGC (DGKE)
XR_001752672.1:n.1055-182_1055-181delinsGC (DGKE)
XR_002958079.1:n.1053-182_1053-181delinsGC (DGKE)
NM_003647.3:c.889-182_889-181delinsGC (DGKE) MANE Select NP_003638.1:n.889-182_889-181delinsGC