Canonical Allele Identifier: CA399905685

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856586G>C , CM000679.2:g.56856586G>C GRCh38
NC_000017.10:g.54933947G>C , CM000679.1:g.54933947G>C GRCh37
NC_000017.9:g.52288946G>C NCBI36
NG_033888.1:g.27488G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682766.1:c.1364-1476C>G (TRIM25) ENSP00000507876.1:n.1364-1476C>G
ENST00000284061.8:c.1173G>C (DGKE) MANE Select ENSP00000284061.3:p.Glu391Asp
ENST00000648772.1:c.1364-1476C>G (TRIM25) ENSP00000498158.1:n.1364-1476C>G
ENST00000284061.7:c.1173G>C (DGKE) ENSP00000284061.3:p.Glu391Asp
ENST00000572944.1:c.1003G>C (DGKE)
NM_003647.2:c.1173G>C (DGKE) NP_003638.1:p.Glu391Asp
XM_011525394.1:c.1227G>C (DGKE) XP_011523696.1:p.Glu409Asp
XM_011525395.1:c.1227G>C (DGKE) XP_011523697.1:p.Glu409Asp
XM_011525396.1:c.1227G>C (DGKE) XP_011523698.1:p.Glu409Asp
XM_011525397.1:c.1227G>C (DGKE) XP_011523699.1:p.Glu409Asp
XM_011525398.1:c.717G>C (DGKE) XP_011523700.1:p.Glu239Asp
XR_934581.1:n.1326G>C (DGKE)
XM_011525394.3:c.1227G>C (DGKE) XP_011523696.1:p.Glu409Asp
XM_011525395.2:c.1227G>C (DGKE) XP_011523697.1:p.Glu409Asp
XM_011525396.2:c.1227G>C (DGKE) XP_011523698.1:p.Glu409Asp
XM_017025243.2:c.1545G>C (DGKE) XP_016880732.1:p.Glu515Asp
XM_017025244.2:c.1227G>C (DGKE) XP_016880733.1:p.Glu409Asp
XR_001752670.2:n.1731G>C (DGKE)
XR_001752671.1:n.1338G>C (DGKE)
XR_001752672.1:n.1339G>C (DGKE)
XR_002958079.1:n.1337G>C (DGKE)
NM_003647.3:c.1173G>C (DGKE) MANE Select NP_003638.1:p.Glu391Asp