Canonical Allele Identifier: CA2267001099

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56861882G= , CM000679.2:g.56861882G= GRCh38
NC_000017.10:g.54939243G= , CM000679.1:g.54939243G= GRCh37
NC_000017.9:g.52294242G= NCBI36
NG_033888.1:g.32784G=

Transcript Alleles

HGVS Amino-acid Change
NM_003647.3:c.1376G= (DGKE) MANE Select NP_003638.1:p.Trp459=
ENST00000284061.8:c.1376G= (DGKE) MANE Select ENSP00000284061.3:p.Trp459=
NM_003647.2:c.1376G= (DGKE) NP_003638.1:p.Trp459=
ENST00000284061.7:c.1376G= (DGKE) ENSP00000284061.3:p.Trp459=
ENST00000572944.1:c.1206G= (DGKE)
ENST00000648772.1:c.1364-6772C= (TRIM25) ENSP00000498158.1:n.1364-6772C=
ENST00000682766.1:c.1364-6772C= (TRIM25) ENSP00000507876.1:n.1364-6772C=
XM_011525394.1:c.1430G= (DGKE) XP_011523696.1:p.Trp477=
XM_011525394.3:c.1430G= (DGKE) XP_011523696.1:p.Trp477=
XM_011525395.1:c.1430G= (DGKE) XP_011523697.1:p.Trp477=
XM_011525395.2:c.1430G= (DGKE) XP_011523697.1:p.Trp477=
XM_011525396.1:c.*67G= (DGKE) XP_011523698.1:n.*67G=
XM_011525396.2:c.*67G= (DGKE) XP_011523698.1:n.*67G=
XM_011525398.1:c.920G= (DGKE) XP_011523700.1:p.Trp307=
XM_017025243.2:c.1748G= (DGKE) XP_016880732.1:p.Trp583=
XM_017025244.2:c.1358G= (DGKE) XP_016880733.1:p.Trp453=
XR_001752670.2:n.1974G= (DGKE)
XR_002958079.1:n.1580G= (DGKE)