Canonical Allele Identifier: CA8663621
Community Standard Title: NM_003647.3(DGKE):c.798T>A (p.Leu266=)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56847975T>A , CM000679.2:g.56847975T>A GRCh38
NC_000017.10:g.54925336T>A , CM000679.1:g.54925336T>A GRCh37
NC_000017.9:g.52280335T>A NCBI36
NG_033888.1:g.18877T>A

Transcript Alleles

HGVS Amino-acid Change
NM_003647.3:c.798T>A (DGKE) MANE Select NP_003638.1:p.Leu266=
ENST00000284061.8:c.798T>A (DGKE) MANE Select ENSP00000284061.3:p.Leu266=
NM_003647.2:c.798T>A (DGKE) NP_003638.1:p.Leu266=
ENST00000284061.7:c.798T>A (DGKE) ENSP00000284061.3:p.Leu266=
ENST00000572944.1:c.628T>A (DGKE)
ENST00000648772.1:c.*313+3968A>T (TRIM25) ENSP00000498158.1:n.*313+3968A>T
XM_011525394.1:c.852T>A (DGKE) XP_011523696.1:p.Leu284=
XM_011525394.3:c.852T>A (DGKE) XP_011523696.1:p.Leu284=
XM_011525395.1:c.852T>A (DGKE) XP_011523697.1:p.Leu284=
XM_011525395.2:c.852T>A (DGKE) XP_011523697.1:p.Leu284=
XM_011525396.1:c.852T>A (DGKE) XP_011523698.1:p.Leu284=
XM_011525396.2:c.852T>A (DGKE) XP_011523698.1:p.Leu284=
XM_011525397.1:c.852T>A (DGKE) XP_011523699.1:p.Leu284=
XM_011525398.1:c.342T>A (DGKE) XP_011523700.1:p.Leu114=
XM_017025243.2:c.798T>A (DGKE) XP_016880732.1:p.Leu266=
XM_017025244.2:c.852T>A (DGKE) XP_016880733.1:p.Leu284=
XR_001752670.2:n.984T>A (DGKE)
XR_001752671.1:n.963T>A (DGKE)
XR_001752672.1:n.964T>A (DGKE)
XR_002958079.1:n.962T>A (DGKE)
XR_934581.1:n.951T>A (DGKE)