Canonical Allele Identifier: CA399927721

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848712T>C , CM000679.2:g.56848712T>C GRCh38
NC_000017.10:g.54926073T>C , CM000679.1:g.54926073T>C GRCh37
NC_000017.9:g.52281072T>C NCBI36
NG_033888.1:g.19614T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.905T>C (DGKE) MANE Select ENSP00000284061.3:p.Ile302Thr
ENST00000648772.1:c.*313+3231A>G (TRIM25) ENSP00000498158.1:n.*313+3231A>G
ENST00000284061.7:c.905T>C (DGKE) ENSP00000284061.3:p.Ile302Thr
ENST00000572944.1:c.735T>C (DGKE)
NM_003647.2:c.905T>C (DGKE) NP_003638.1:p.Ile302Thr
XM_011525394.1:c.959T>C (DGKE) XP_011523696.1:p.Ile320Thr
XM_011525395.1:c.959T>C (DGKE) XP_011523697.1:p.Ile320Thr
XM_011525396.1:c.959T>C (DGKE) XP_011523698.1:p.Ile320Thr
XM_011525397.1:c.959T>C (DGKE) XP_011523699.1:p.Ile320Thr
XM_011525398.1:c.449T>C (DGKE) XP_011523700.1:p.Ile150Thr
XR_934581.1:n.1058T>C (DGKE)
XM_011525394.3:c.959T>C (DGKE) XP_011523696.1:p.Ile320Thr
XM_011525395.2:c.959T>C (DGKE) XP_011523697.1:p.Ile320Thr
XM_011525396.2:c.959T>C (DGKE) XP_011523698.1:p.Ile320Thr
XM_017025243.2:c.1277T>C (DGKE) XP_016880732.1:p.Ile426Thr
XM_017025244.2:c.959T>C (DGKE) XP_016880733.1:p.Ile320Thr
XR_001752670.2:n.1463T>C (DGKE)
XR_001752671.1:n.1070T>C (DGKE)
XR_001752672.1:n.1071T>C (DGKE)
XR_002958079.1:n.1069T>C (DGKE)
NM_003647.3:c.905T>C (DGKE) MANE Select NP_003638.1:p.Ile302Thr