Canonical Allele Identifier: CA399927841

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848745G>C , CM000679.2:g.56848745G>C GRCh38
NC_000017.10:g.54926106G>C , CM000679.1:g.54926106G>C GRCh37
NC_000017.9:g.52281105G>C NCBI36
NG_033888.1:g.19647G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.938G>C (DGKE) MANE Select ENSP00000284061.3:p.Gly313Ala
ENST00000648772.1:c.*313+3198C>G (TRIM25) ENSP00000498158.1:n.*313+3198C>G
ENST00000284061.7:c.938G>C (DGKE) ENSP00000284061.3:p.Gly313Ala
ENST00000572944.1:c.768G>C (DGKE)
NM_003647.2:c.938G>C (DGKE) NP_003638.1:p.Gly313Ala
XM_011525394.1:c.992G>C (DGKE) XP_011523696.1:p.Gly331Ala
XM_011525395.1:c.992G>C (DGKE) XP_011523697.1:p.Gly331Ala
XM_011525396.1:c.992G>C (DGKE) XP_011523698.1:p.Gly331Ala
XM_011525397.1:c.992G>C (DGKE) XP_011523699.1:p.Gly331Ala
XM_011525398.1:c.482G>C (DGKE) XP_011523700.1:p.Gly161Ala
XR_934581.1:n.1091G>C (DGKE)
XM_011525394.3:c.992G>C (DGKE) XP_011523696.1:p.Gly331Ala
XM_011525395.2:c.992G>C (DGKE) XP_011523697.1:p.Gly331Ala
XM_011525396.2:c.992G>C (DGKE) XP_011523698.1:p.Gly331Ala
XM_017025243.2:c.1310G>C (DGKE) XP_016880732.1:p.Gly437Ala
XM_017025244.2:c.992G>C (DGKE) XP_016880733.1:p.Gly331Ala
XR_001752670.2:n.1496G>C (DGKE)
XR_001752671.1:n.1103G>C (DGKE)
XR_001752672.1:n.1104G>C (DGKE)
XR_002958079.1:n.1102G>C (DGKE)
NM_003647.3:c.938G>C (DGKE) MANE Select NP_003638.1:p.Gly313Ala