Canonical Allele Identifier: CA2266995228

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56849025A= , CM000679.2:g.56849025A= GRCh38
NC_000017.10:g.54926386A= , CM000679.1:g.54926386A= GRCh37
NC_000017.9:g.52281385A= NCBI36
NG_033888.1:g.19927A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1047-156A= (DGKE) MANE Select ENSP00000284061.3:n.1047-156A=
ENST00000648772.1:c.*313+2918T= (TRIM25) ENSP00000498158.1:n.*313+2918T=
ENST00000284061.7:c.1047-156A= (DGKE) ENSP00000284061.3:n.1047-156A=
ENST00000572944.1:c.877-156A= (DGKE)
NM_003647.2:c.1047-156A= (DGKE) NP_003638.1:n.1047-156A=
XM_011525394.1:c.1101-156A= (DGKE) XP_011523696.1:n.1101-156A=
XM_011525395.1:c.1101-156A= (DGKE) XP_011523697.1:n.1101-156A=
XM_011525396.1:c.1101-156A= (DGKE) XP_011523698.1:n.1101-156A=
XM_011525397.1:c.1101-156A= (DGKE) XP_011523699.1:n.1101-156A=
XM_011525398.1:c.591-156A= (DGKE) XP_011523700.1:n.591-156A=
XR_934581.1:n.1200-156A= (DGKE)
XM_011525394.3:c.1101-156A= (DGKE) XP_011523696.1:n.1101-156A=
XM_011525395.2:c.1101-156A= (DGKE) XP_011523697.1:n.1101-156A=
XM_011525396.2:c.1101-156A= (DGKE) XP_011523698.1:n.1101-156A=
XM_017025243.2:c.1419-156A= (DGKE) XP_016880732.1:n.1419-156A=
XM_017025244.2:c.1101-156A= (DGKE) XP_016880733.1:n.1101-156A=
XR_001752670.2:n.1605-156A= (DGKE)
XR_001752671.1:n.1212-156A= (DGKE)
XR_001752672.1:n.1213-156A= (DGKE)
XR_002958079.1:n.1211-156A= (DGKE)
NM_003647.3:c.1047-156A= (DGKE) MANE Select NP_003638.1:n.1047-156A=