Canonical Allele Identifier: CA2638885529

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843962_56843963del , CM000679.2:g.56843962_56843963del GRCh38
NC_000017.10:g.54921323_54921324del , CM000679.1:g.54921323_54921324del GRCh37
NC_000017.9:g.52276322_52276323del NCBI36
NG_033888.1:g.14864_14865del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.465-57_465-56del (DGKE) MANE Select ENSP00000284061.3:n.465-57_465-56del
ENST00000648772.1:c.*314-173_*314-172del (TRIM25) ENSP00000498158.1:n.*314-173_*314-172del
ENST00000284061.7:c.465-57_465-56del (DGKE) ENSP00000284061.3:n.465-57_465-56del
ENST00000572944.1:c.295-57_295-56del (DGKE)
ENST00000576869.5:n.613-57_613-56del (DGKE)
NM_003647.2:c.465-57_465-56del (DGKE) NP_003638.1:n.465-57_465-56del
XM_011525394.1:c.519-57_519-56del (DGKE) XP_011523696.1:n.519-57_519-56del
XM_011525395.1:c.519-57_519-56del (DGKE) XP_011523697.1:n.519-57_519-56del
XM_011525396.1:c.519-57_519-56del (DGKE) XP_011523698.1:n.519-57_519-56del
XM_011525397.1:c.519-57_519-56del (DGKE) XP_011523699.1:n.519-57_519-56del
XM_011525398.1:c.8+55_9-56del (DGKE) XP_011523700.1:n.8+55_9-56del
XR_934581.1:n.618-57_618-56del (DGKE)
XM_011525394.3:c.519-57_519-56del (DGKE) XP_011523696.1:n.519-57_519-56del
XM_011525395.2:c.519-57_519-56del (DGKE) XP_011523697.1:n.519-57_519-56del
XM_011525396.2:c.519-57_519-56del (DGKE) XP_011523698.1:n.519-57_519-56del
XM_017025243.2:c.465-57_465-56del (DGKE) XP_016880732.1:n.465-57_465-56del
XM_017025244.2:c.519-57_519-56del (DGKE) XP_016880733.1:n.519-57_519-56del
XR_001752670.2:n.651-57_651-56del (DGKE)
XR_001752671.1:n.630-57_630-56del (DGKE)
XR_001752672.1:n.631-57_631-56del (DGKE)
XR_002958079.1:n.629-57_629-56del (DGKE)
NM_003647.3:c.465-57_465-56del (DGKE) MANE Select NP_003638.1:n.465-57_465-56del