Canonical Allele Identifier: CA2638885527

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843960_56843961insAAA , CM000679.2:g.56843960_56843961insAAA GRCh38
NC_000017.10:g.54921321_54921322insAAA , CM000679.1:g.54921321_54921322insAAA GRCh37
NC_000017.9:g.52276320_52276321insAAA NCBI36
NG_033888.1:g.14862_14863insAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.465-59_465-58insAAA (DGKE) MANE Select ENSP00000284061.3:n.465-59_465-58insAAA
ENST00000648772.1:c.*314-171_*314-170insTTT (TRIM25) ENSP00000498158.1:n.*314-171_*314-170insTTT
ENST00000284061.7:c.465-59_465-58insAAA (DGKE) ENSP00000284061.3:n.465-59_465-58insAAA
ENST00000572944.1:c.295-59_295-58insAAA (DGKE)
ENST00000576869.5:n.613-59_613-58insAAA (DGKE)
NM_003647.2:c.465-59_465-58insAAA (DGKE) NP_003638.1:n.465-59_465-58insAAA
XM_011525394.1:c.519-59_519-58insAAA (DGKE) XP_011523696.1:n.519-59_519-58insAAA
XM_011525395.1:c.519-59_519-58insAAA (DGKE) XP_011523697.1:n.519-59_519-58insAAA
XM_011525396.1:c.519-59_519-58insAAA (DGKE) XP_011523698.1:n.519-59_519-58insAAA
XM_011525397.1:c.519-59_519-58insAAA (DGKE) XP_011523699.1:n.519-59_519-58insAAA
XM_011525398.1:c.8+53_8+54insAAA (DGKE) XP_011523700.1:n.8+53_8+54insAAA
XR_934581.1:n.618-59_618-58insAAA (DGKE)
XM_011525394.3:c.519-59_519-58insAAA (DGKE) XP_011523696.1:n.519-59_519-58insAAA
XM_011525395.2:c.519-59_519-58insAAA (DGKE) XP_011523697.1:n.519-59_519-58insAAA
XM_011525396.2:c.519-59_519-58insAAA (DGKE) XP_011523698.1:n.519-59_519-58insAAA
XM_017025243.2:c.465-59_465-58insAAA (DGKE) XP_016880732.1:n.465-59_465-58insAAA
XM_017025244.2:c.519-59_519-58insAAA (DGKE) XP_016880733.1:n.519-59_519-58insAAA
XR_001752670.2:n.651-59_651-58insAAA (DGKE)
XR_001752671.1:n.630-59_630-58insAAA (DGKE)
XR_001752672.1:n.631-59_631-58insAAA (DGKE)
XR_002958079.1:n.629-59_629-58insAAA (DGKE)
NM_003647.3:c.465-59_465-58insAAA (DGKE) MANE Select NP_003638.1:n.465-59_465-58insAAA