Canonical Allele Identifier: CA2266995080

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848658_56848660delinsCTG , CM000679.2:g.56848658_56848660delinsCTG GRCh38
NC_000017.10:g.54926019_54926021delinsCTG , CM000679.1:g.54926019_54926021delinsCTG GRCh37
NC_000017.9:g.52281018_52281020delinsCTG NCBI36
NG_033888.1:g.19560_19562delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.889-38_889-36delinsCTG (DGKE) MANE Select ENSP00000284061.3:n.889-38_889-36delinsCT...
ENST00000648772.1:c.*313+3283_*313+3285delinsCAG (TRIM25) ENSP00000498158.1:n.*313+3283_*313+3285de...
ENST00000284061.7:c.889-38_889-36delinsCTG (DGKE) ENSP00000284061.3:n.889-38_889-36delinsCT...
ENST00000572944.1:c.719-38_719-36delinsCTG (DGKE)
NM_003647.2:c.889-38_889-36delinsCTG (DGKE) NP_003638.1:n.889-38_889-36delinsCTG
XM_011525394.1:c.943-38_943-36delinsCTG (DGKE) XP_011523696.1:n.943-38_943-36delinsCTG
XM_011525395.1:c.943-38_943-36delinsCTG (DGKE) XP_011523697.1:n.943-38_943-36delinsCTG
XM_011525396.1:c.943-38_943-36delinsCTG (DGKE) XP_011523698.1:n.943-38_943-36delinsCTG
XM_011525397.1:c.943-38_943-36delinsCTG (DGKE) XP_011523699.1:n.943-38_943-36delinsCTG
XM_011525398.1:c.433-38_433-36delinsCTG (DGKE) XP_011523700.1:n.433-38_433-36delinsCTG
XR_934581.1:n.1042-38_1042-36delinsCTG (DGKE)
XM_011525394.3:c.943-38_943-36delinsCTG (DGKE) XP_011523696.1:n.943-38_943-36delinsCTG
XM_011525395.2:c.943-38_943-36delinsCTG (DGKE) XP_011523697.1:n.943-38_943-36delinsCTG
XM_011525396.2:c.943-38_943-36delinsCTG (DGKE) XP_011523698.1:n.943-38_943-36delinsCTG
XM_017025243.2:c.1261-38_1261-36delinsCTG (DGKE) XP_016880732.1:n.1261-38_1261-36delinsCTG...
XM_017025244.2:c.943-38_943-36delinsCTG (DGKE) XP_016880733.1:n.943-38_943-36delinsCTG
XR_001752670.2:n.1447-38_1447-36delinsCTG (DGKE)
XR_001752671.1:n.1054-38_1054-36delinsCTG (DGKE)
XR_001752672.1:n.1055-38_1055-36delinsCTG (DGKE)
XR_002958079.1:n.1053-38_1053-36delinsCTG (DGKE)
NM_003647.3:c.889-38_889-36delinsCTG (DGKE) MANE Select NP_003638.1:n.889-38_889-36delinsCTG