Canonical Allele Identifier: CA500687142

Linked Data

MyVariant Identifiers: chr17:g.54926074T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848713T>A , CM000679.2:g.56848713T>A GRCh38
NC_000017.10:g.54926074T>A , CM000679.1:g.54926074T>A GRCh37
NC_000017.9:g.52281073T>A NCBI36
NG_033888.1:g.19615T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.906T>A (DGKE) MANE Select ENSP00000284061.3:p.Ile302=
ENST00000648772.1:c.*313+3230A>T (TRIM25) ENSP00000498158.1:n.*313+3230A>T
ENST00000284061.7:c.906T>A (DGKE) ENSP00000284061.3:p.Ile302=
ENST00000572944.1:c.736T>A (DGKE)
NM_003647.2:c.906T>A (DGKE) NP_003638.1:p.Ile302=
XM_011525394.1:c.960T>A (DGKE) XP_011523696.1:p.Ile320=
XM_011525395.1:c.960T>A (DGKE) XP_011523697.1:p.Ile320=
XM_011525396.1:c.960T>A (DGKE) XP_011523698.1:p.Ile320=
XM_011525397.1:c.960T>A (DGKE) XP_011523699.1:p.Ile320=
XM_011525398.1:c.450T>A (DGKE) XP_011523700.1:p.Ile150=
XR_934581.1:n.1059T>A (DGKE)
XM_011525394.3:c.960T>A (DGKE) XP_011523696.1:p.Ile320=
XM_011525395.2:c.960T>A (DGKE) XP_011523697.1:p.Ile320=
XM_011525396.2:c.960T>A (DGKE) XP_011523698.1:p.Ile320=
XM_017025243.2:c.1278T>A (DGKE) XP_016880732.1:p.Ile426=
XM_017025244.2:c.960T>A (DGKE) XP_016880733.1:p.Ile320=
XR_001752670.2:n.1464T>A (DGKE)
XR_001752671.1:n.1071T>A (DGKE)
XR_001752672.1:n.1072T>A (DGKE)
XR_002958079.1:n.1070T>A (DGKE)
NM_003647.3:c.906T>A (DGKE) MANE Select NP_003638.1:p.Ile302=