Canonical Allele Identifier: CA399925943

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56844041G>C , CM000679.2:g.56844041G>C GRCh38
NC_000017.10:g.54921402G>C , CM000679.1:g.54921402G>C GRCh37
NC_000017.9:g.52276401G>C NCBI36
NG_033888.1:g.14943G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.487G>C (DGKE) MANE Select ENSP00000284061.3:p.Val163Leu
ENST00000648772.1:c.*314-251C>G (TRIM25) ENSP00000498158.1:n.*314-251C>G
ENST00000284061.7:c.487G>C (DGKE) ENSP00000284061.3:p.Val163Leu
ENST00000571084.1:n.23G>C (DGKE)
ENST00000572944.1:c.317G>C (DGKE)
ENST00000576869.5:n.635G>C (DGKE)
NM_003647.2:c.487G>C (DGKE) NP_003638.1:p.Val163Leu
XM_011525394.1:c.541G>C (DGKE) XP_011523696.1:p.Val181Leu
XM_011525395.1:c.541G>C (DGKE) XP_011523697.1:p.Val181Leu
XM_011525396.1:c.541G>C (DGKE) XP_011523698.1:p.Val181Leu
XM_011525397.1:c.541G>C (DGKE) XP_011523699.1:p.Val181Leu
XM_011525398.1:c.31G>C (DGKE) XP_011523700.1:p.Val11Leu
XR_934581.1:n.640G>C (DGKE)
XM_011525394.3:c.541G>C (DGKE) XP_011523696.1:p.Val181Leu
XM_011525395.2:c.541G>C (DGKE) XP_011523697.1:p.Val181Leu
XM_011525396.2:c.541G>C (DGKE) XP_011523698.1:p.Val181Leu
XM_017025243.2:c.487G>C (DGKE) XP_016880732.1:p.Val163Leu
XM_017025244.2:c.541G>C (DGKE) XP_016880733.1:p.Val181Leu
XR_001752670.2:n.673G>C (DGKE)
XR_001752671.1:n.652G>C (DGKE)
XR_001752672.1:n.653G>C (DGKE)
XR_002958079.1:n.651G>C (DGKE)
NM_003647.3:c.487G>C (DGKE) MANE Select NP_003638.1:p.Val163Leu