Canonical Allele Identifier: CA773366495

Linked Data

dbSNP Id: rs1192374669

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843959dup , CM000679.2:g.56843959dup GRCh38
NC_000017.10:g.54921320dup , CM000679.1:g.54921320dup GRCh37
NC_000017.9:g.52276319dup NCBI36
NG_033888.1:g.14861dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.465-60dup (DGKE) MANE Select ENSP00000284061.3:n.465-60dup
ENST00000648772.1:c.*314-169dup (TRIM25) ENSP00000498158.1:n.*314-169dup
ENST00000284061.7:c.465-60dup (DGKE) ENSP00000284061.3:n.465-60dup
ENST00000572944.1:c.295-60dup (DGKE)
ENST00000576869.5:n.613-60dup (DGKE)
NM_003647.2:c.465-60dup (DGKE) NP_003638.1:n.465-60dup
XM_011525394.1:c.519-60dup (DGKE) XP_011523696.1:n.519-60dup
XM_011525395.1:c.519-60dup (DGKE) XP_011523697.1:n.519-60dup
XM_011525396.1:c.519-60dup (DGKE) XP_011523698.1:n.519-60dup
XM_011525397.1:c.519-60dup (DGKE) XP_011523699.1:n.519-60dup
XM_011525398.1:c.8+52dup (DGKE) XP_011523700.1:n.8+52dup
XR_934581.1:n.618-60dup (DGKE)
XM_011525394.3:c.519-60dup (DGKE) XP_011523696.1:n.519-60dup
XM_011525395.2:c.519-60dup (DGKE) XP_011523697.1:n.519-60dup
XM_011525396.2:c.519-60dup (DGKE) XP_011523698.1:n.519-60dup
XM_017025243.2:c.465-60dup (DGKE) XP_016880732.1:n.465-60dup
XM_017025244.2:c.519-60dup (DGKE) XP_016880733.1:n.519-60dup
XR_001752670.2:n.651-60dup (DGKE)
XR_001752671.1:n.630-60dup (DGKE)
XR_001752672.1:n.631-60dup (DGKE)
XR_002958079.1:n.629-60dup (DGKE)
NM_003647.3:c.465-60dup (DGKE) MANE Select NP_003638.1:n.465-60dup