Canonical Allele Identifier: CA399925907

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56844027G>C , CM000679.2:g.56844027G>C GRCh38
NC_000017.10:g.54921388G>C , CM000679.1:g.54921388G>C GRCh37
NC_000017.9:g.52276387G>C NCBI36
NG_033888.1:g.14929G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.473G>C (DGKE) MANE Select ENSP00000284061.3:p.Trp158Ser
ENST00000648772.1:c.*314-237C>G (TRIM25) ENSP00000498158.1:n.*314-237C>G
ENST00000284061.7:c.473G>C (DGKE) ENSP00000284061.3:p.Trp158Ser
ENST00000571084.1:n.9G>C (DGKE)
ENST00000572944.1:c.303G>C (DGKE)
ENST00000576869.5:n.621G>C (DGKE)
NM_003647.2:c.473G>C (DGKE) NP_003638.1:p.Trp158Ser
XM_011525394.1:c.527G>C (DGKE) XP_011523696.1:p.Trp176Ser
XM_011525395.1:c.527G>C (DGKE) XP_011523697.1:p.Trp176Ser
XM_011525396.1:c.527G>C (DGKE) XP_011523698.1:p.Trp176Ser
XM_011525397.1:c.527G>C (DGKE) XP_011523699.1:p.Trp176Ser
XM_011525398.1:c.17G>C (DGKE) XP_011523700.1:p.Trp6Ser
XR_934581.1:n.626G>C (DGKE)
XM_011525394.3:c.527G>C (DGKE) XP_011523696.1:p.Trp176Ser
XM_011525395.2:c.527G>C (DGKE) XP_011523697.1:p.Trp176Ser
XM_011525396.2:c.527G>C (DGKE) XP_011523698.1:p.Trp176Ser
XM_017025243.2:c.473G>C (DGKE) XP_016880732.1:p.Trp158Ser
XM_017025244.2:c.527G>C (DGKE) XP_016880733.1:p.Trp176Ser
XR_001752670.2:n.659G>C (DGKE)
XR_001752671.1:n.638G>C (DGKE)
XR_001752672.1:n.639G>C (DGKE)
XR_002958079.1:n.637G>C (DGKE)
NM_003647.3:c.473G>C (DGKE) MANE Select NP_003638.1:p.Trp158Ser