Canonical Allele Identifier: CA2266998653

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856483C= , CM000679.2:g.56856483C= GRCh38
NC_000017.10:g.54933844C= , CM000679.1:g.54933844C= GRCh37
NC_000017.9:g.52288843C= NCBI36
NG_033888.1:g.27385C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1373G= (TRIM25) ENSP00000507876.1:n.1364-1373G=
ENST00000284061.8:c.1099-29C= (DGKE) MANE Select ENSP00000284061.3:n.1099-29C=
ENST00000648772.1:c.1364-1373G= (TRIM25) ENSP00000498158.1:n.1364-1373G=
ENST00000284061.7:c.1099-29C= (DGKE) ENSP00000284061.3:n.1099-29C=
ENST00000572944.1:c.929-29C= (DGKE)
NM_003647.2:c.1099-29C= (DGKE) NP_003638.1:n.1099-29C=
XM_011525394.1:c.1153-29C= (DGKE) XP_011523696.1:n.1153-29C=
XM_011525395.1:c.1153-29C= (DGKE) XP_011523697.1:n.1153-29C=
XM_011525396.1:c.1153-29C= (DGKE) XP_011523698.1:n.1153-29C=
XM_011525397.1:c.1153-29C= (DGKE) XP_011523699.1:n.1153-29C=
XM_011525398.1:c.643-29C= (DGKE) XP_011523700.1:n.643-29C=
XR_934581.1:n.1252-29C= (DGKE)
XM_011525394.3:c.1153-29C= (DGKE) XP_011523696.1:n.1153-29C=
XM_011525395.2:c.1153-29C= (DGKE) XP_011523697.1:n.1153-29C=
XM_011525396.2:c.1153-29C= (DGKE) XP_011523698.1:n.1153-29C=
XM_017025243.2:c.1471-29C= (DGKE) XP_016880732.1:n.1471-29C=
XM_017025244.2:c.1153-29C= (DGKE) XP_016880733.1:n.1153-29C=
XR_001752670.2:n.1657-29C= (DGKE)
XR_001752671.1:n.1264-29C= (DGKE)
XR_001752672.1:n.1265-29C= (DGKE)
XR_002958079.1:n.1263-29C= (DGKE)
NM_003647.3:c.1099-29C= (DGKE) MANE Select NP_003638.1:n.1099-29C=