Canonical Allele Identifier: CA399905543

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856528A>T , CM000679.2:g.56856528A>T GRCh38
NC_000017.10:g.54933889A>T , CM000679.1:g.54933889A>T GRCh37
NC_000017.9:g.52288888A>T NCBI36
NG_033888.1:g.27430A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1418T>A (TRIM25) ENSP00000507876.1:n.1364-1418T>A
ENST00000284061.8:c.1115A>T (DGKE) MANE Select ENSP00000284061.3:p.Asn372Ile
ENST00000648772.1:c.1364-1418T>A (TRIM25) ENSP00000498158.1:n.1364-1418T>A
ENST00000284061.7:c.1115A>T (DGKE) ENSP00000284061.3:p.Asn372Ile
ENST00000572944.1:c.945A>T (DGKE)
NM_003647.2:c.1115A>T (DGKE) NP_003638.1:p.Asn372Ile
XM_011525394.1:c.1169A>T (DGKE) XP_011523696.1:p.Asn390Ile
XM_011525395.1:c.1169A>T (DGKE) XP_011523697.1:p.Asn390Ile
XM_011525396.1:c.1169A>T (DGKE) XP_011523698.1:p.Asn390Ile
XM_011525397.1:c.1169A>T (DGKE) XP_011523699.1:p.Asn390Ile
XM_011525398.1:c.659A>T (DGKE) XP_011523700.1:p.Asn220Ile
XR_934581.1:n.1268A>T (DGKE)
XM_011525394.3:c.1169A>T (DGKE) XP_011523696.1:p.Asn390Ile
XM_011525395.2:c.1169A>T (DGKE) XP_011523697.1:p.Asn390Ile
XM_011525396.2:c.1169A>T (DGKE) XP_011523698.1:p.Asn390Ile
XM_017025243.2:c.1487A>T (DGKE) XP_016880732.1:p.Asn496Ile
XM_017025244.2:c.1169A>T (DGKE) XP_016880733.1:p.Asn390Ile
XR_001752670.2:n.1673A>T (DGKE)
XR_001752671.1:n.1280A>T (DGKE)
XR_001752672.1:n.1281A>T (DGKE)
XR_002958079.1:n.1279A>T (DGKE)
NM_003647.3:c.1115A>T (DGKE) MANE Select NP_003638.1:p.Asn372Ile