Canonical Allele Identifier: CA2638885520

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843954T>C , CM000679.2:g.56843954T>C GRCh38
NC_000017.10:g.54921315T>C , CM000679.1:g.54921315T>C GRCh37
NC_000017.9:g.52276314T>C NCBI36
NG_033888.1:g.14856T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.465-65T>C (DGKE) MANE Select ENSP00000284061.3:n.465-65T>C
ENST00000648772.1:c.*314-164A>G (TRIM25) ENSP00000498158.1:n.*314-164A>G
ENST00000284061.7:c.465-65T>C (DGKE) ENSP00000284061.3:n.465-65T>C
ENST00000572944.1:c.295-65T>C (DGKE)
ENST00000576869.5:n.613-65T>C (DGKE)
NM_003647.2:c.465-65T>C (DGKE) NP_003638.1:n.465-65T>C
XM_011525394.1:c.519-65T>C (DGKE) XP_011523696.1:n.519-65T>C
XM_011525395.1:c.519-65T>C (DGKE) XP_011523697.1:n.519-65T>C
XM_011525396.1:c.519-65T>C (DGKE) XP_011523698.1:n.519-65T>C
XM_011525397.1:c.519-65T>C (DGKE) XP_011523699.1:n.519-65T>C
XM_011525398.1:c.8+47T>C (DGKE) XP_011523700.1:n.8+47T>C
XR_934581.1:n.618-65T>C (DGKE)
XM_011525394.3:c.519-65T>C (DGKE) XP_011523696.1:n.519-65T>C
XM_011525395.2:c.519-65T>C (DGKE) XP_011523697.1:n.519-65T>C
XM_011525396.2:c.519-65T>C (DGKE) XP_011523698.1:n.519-65T>C
XM_017025243.2:c.465-65T>C (DGKE) XP_016880732.1:n.465-65T>C
XM_017025244.2:c.519-65T>C (DGKE) XP_016880733.1:n.519-65T>C
XR_001752670.2:n.651-65T>C (DGKE)
XR_001752671.1:n.630-65T>C (DGKE)
XR_001752672.1:n.631-65T>C (DGKE)
XR_002958079.1:n.629-65T>C (DGKE)
NM_003647.3:c.465-65T>C (DGKE) MANE Select NP_003638.1:n.465-65T>C