Canonical Allele Identifier: CA2638885519

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843953G>T , CM000679.2:g.56843953G>T GRCh38
NC_000017.10:g.54921314G>T , CM000679.1:g.54921314G>T GRCh37
NC_000017.9:g.52276313G>T NCBI36
NG_033888.1:g.14855G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.465-66G>T (DGKE) MANE Select ENSP00000284061.3:n.465-66G>T
ENST00000648772.1:c.*314-163C>A (TRIM25) ENSP00000498158.1:n.*314-163C>A
ENST00000284061.7:c.465-66G>T (DGKE) ENSP00000284061.3:n.465-66G>T
ENST00000572944.1:c.295-66G>T (DGKE)
ENST00000576869.5:n.613-66G>T (DGKE)
NM_003647.2:c.465-66G>T (DGKE) NP_003638.1:n.465-66G>T
XM_011525394.1:c.519-66G>T (DGKE) XP_011523696.1:n.519-66G>T
XM_011525395.1:c.519-66G>T (DGKE) XP_011523697.1:n.519-66G>T
XM_011525396.1:c.519-66G>T (DGKE) XP_011523698.1:n.519-66G>T
XM_011525397.1:c.519-66G>T (DGKE) XP_011523699.1:n.519-66G>T
XM_011525398.1:c.8+46G>T (DGKE) XP_011523700.1:n.8+46G>T
XR_934581.1:n.618-66G>T (DGKE)
XM_011525394.3:c.519-66G>T (DGKE) XP_011523696.1:n.519-66G>T
XM_011525395.2:c.519-66G>T (DGKE) XP_011523697.1:n.519-66G>T
XM_011525396.2:c.519-66G>T (DGKE) XP_011523698.1:n.519-66G>T
XM_017025243.2:c.465-66G>T (DGKE) XP_016880732.1:n.465-66G>T
XM_017025244.2:c.519-66G>T (DGKE) XP_016880733.1:n.519-66G>T
XR_001752670.2:n.651-66G>T (DGKE)
XR_001752671.1:n.630-66G>T (DGKE)
XR_001752672.1:n.631-66G>T (DGKE)
XR_002958079.1:n.629-66G>T (DGKE)
NM_003647.3:c.465-66G>T (DGKE) MANE Select NP_003638.1:n.465-66G>T