Canonical Allele Identifier: CA399927824

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848736T>A , CM000679.2:g.56848736T>A GRCh38
NC_000017.10:g.54926097T>A , CM000679.1:g.54926097T>A GRCh37
NC_000017.9:g.52281096T>A NCBI36
NG_033888.1:g.19638T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.929T>A (DGKE) MANE Select ENSP00000284061.3:p.Leu310Gln
ENST00000648772.1:c.*313+3207A>T (TRIM25) ENSP00000498158.1:n.*313+3207A>T
ENST00000284061.7:c.929T>A (DGKE) ENSP00000284061.3:p.Leu310Gln
ENST00000572944.1:c.759T>A (DGKE)
NM_003647.2:c.929T>A (DGKE) NP_003638.1:p.Leu310Gln
XM_011525394.1:c.983T>A (DGKE) XP_011523696.1:p.Leu328Gln
XM_011525395.1:c.983T>A (DGKE) XP_011523697.1:p.Leu328Gln
XM_011525396.1:c.983T>A (DGKE) XP_011523698.1:p.Leu328Gln
XM_011525397.1:c.983T>A (DGKE) XP_011523699.1:p.Leu328Gln
XM_011525398.1:c.473T>A (DGKE) XP_011523700.1:p.Leu158Gln
XR_934581.1:n.1082T>A (DGKE)
XM_011525394.3:c.983T>A (DGKE) XP_011523696.1:p.Leu328Gln
XM_011525395.2:c.983T>A (DGKE) XP_011523697.1:p.Leu328Gln
XM_011525396.2:c.983T>A (DGKE) XP_011523698.1:p.Leu328Gln
XM_017025243.2:c.1301T>A (DGKE) XP_016880732.1:p.Leu434Gln
XM_017025244.2:c.983T>A (DGKE) XP_016880733.1:p.Leu328Gln
XR_001752670.2:n.1487T>A (DGKE)
XR_001752671.1:n.1094T>A (DGKE)
XR_001752672.1:n.1095T>A (DGKE)
XR_002958079.1:n.1093T>A (DGKE)
NM_003647.3:c.929T>A (DGKE) MANE Select NP_003638.1:p.Leu310Gln