Canonical Allele Identifier: CA399905534

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856526C>G , CM000679.2:g.56856526C>G GRCh38
NC_000017.10:g.54933887C>G , CM000679.1:g.54933887C>G GRCh37
NC_000017.9:g.52288886C>G NCBI36
NG_033888.1:g.27428C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1416G>C (TRIM25) ENSP00000507876.1:n.1364-1416G>C
ENST00000284061.8:c.1113C>G (DGKE) MANE Select ENSP00000284061.3:p.Asn371Lys
ENST00000648772.1:c.1364-1416G>C (TRIM25) ENSP00000498158.1:n.1364-1416G>C
ENST00000284061.7:c.1113C>G (DGKE) ENSP00000284061.3:p.Asn371Lys
ENST00000572944.1:c.943C>G (DGKE)
NM_003647.2:c.1113C>G (DGKE) NP_003638.1:p.Asn371Lys
XM_011525394.1:c.1167C>G (DGKE) XP_011523696.1:p.Asn389Lys
XM_011525395.1:c.1167C>G (DGKE) XP_011523697.1:p.Asn389Lys
XM_011525396.1:c.1167C>G (DGKE) XP_011523698.1:p.Asn389Lys
XM_011525397.1:c.1167C>G (DGKE) XP_011523699.1:p.Asn389Lys
XM_011525398.1:c.657C>G (DGKE) XP_011523700.1:p.Asn219Lys
XR_934581.1:n.1266C>G (DGKE)
XM_011525394.3:c.1167C>G (DGKE) XP_011523696.1:p.Asn389Lys
XM_011525395.2:c.1167C>G (DGKE) XP_011523697.1:p.Asn389Lys
XM_011525396.2:c.1167C>G (DGKE) XP_011523698.1:p.Asn389Lys
XM_017025243.2:c.1485C>G (DGKE) XP_016880732.1:p.Asn495Lys
XM_017025244.2:c.1167C>G (DGKE) XP_016880733.1:p.Asn389Lys
XR_001752670.2:n.1671C>G (DGKE)
XR_001752671.1:n.1278C>G (DGKE)
XR_001752672.1:n.1279C>G (DGKE)
XR_002958079.1:n.1277C>G (DGKE)
NM_003647.3:c.1113C>G (DGKE) MANE Select NP_003638.1:p.Asn371Lys