Canonical Allele Identifier: CA8663653

Linked Data

dbSNP Id: rs756357670

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848717C>G , CM000679.2:g.56848717C>G GRCh38
NC_000017.10:g.54926078C>G , CM000679.1:g.54926078C>G GRCh37
NC_000017.9:g.52281077C>G NCBI36
NG_033888.1:g.19619C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.910C>G (DGKE) MANE Select ENSP00000284061.3:p.Gln304Glu
ENST00000648772.1:c.*313+3226G>C (TRIM25) ENSP00000498158.1:n.*313+3226G>C
ENST00000284061.7:c.910C>G (DGKE) ENSP00000284061.3:p.Gln304Glu
ENST00000572944.1:c.740C>G (DGKE)
NM_003647.2:c.910C>G (DGKE) NP_003638.1:p.Gln304Glu
XM_011525394.1:c.964C>G (DGKE) XP_011523696.1:p.Gln322Glu
XM_011525395.1:c.964C>G (DGKE) XP_011523697.1:p.Gln322Glu
XM_011525396.1:c.964C>G (DGKE) XP_011523698.1:p.Gln322Glu
XM_011525397.1:c.964C>G (DGKE) XP_011523699.1:p.Gln322Glu
XM_011525398.1:c.454C>G (DGKE) XP_011523700.1:p.Gln152Glu
XR_934581.1:n.1063C>G (DGKE)
XM_011525394.3:c.964C>G (DGKE) XP_011523696.1:p.Gln322Glu
XM_011525395.2:c.964C>G (DGKE) XP_011523697.1:p.Gln322Glu
XM_011525396.2:c.964C>G (DGKE) XP_011523698.1:p.Gln322Glu
XM_017025243.2:c.1282C>G (DGKE) XP_016880732.1:p.Gln428Glu
XM_017025244.2:c.964C>G (DGKE) XP_016880733.1:p.Gln322Glu
XR_001752670.2:n.1468C>G (DGKE)
XR_001752671.1:n.1075C>G (DGKE)
XR_001752672.1:n.1076C>G (DGKE)
XR_002958079.1:n.1074C>G (DGKE)
NM_003647.3:c.910C>G (DGKE) MANE Select NP_003638.1:p.Gln304Glu