Canonical Allele Identifier: CA332174
Gene: DGKE HGNC NCBI

Linked Data

ClinVar Variation Id: 135640
dbSNP Id: rs312262696

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848695G>A , CM000679.2:g.56848695G>A GRCh38
NC_000017.10:g.54926056G>A , CM000679.1:g.54926056G>A GRCh37
NC_000017.9:g.52281055G>A NCBI36
NG_033888.1:g.19597G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.889-1G>A MANE Select ENSP00000284061.3:p.=
ENST00000648772.1:c.*313+3248C>T ENSP00000498158.1:p.=
ENST00000284061.7:c.889-1G>A ENSP00000284061.3:p.=
ENST00000572944.1:n.719-1G>A
NM_003647.2:c.889-1G>A NP_003638.1:p.=
XM_011525394.1:c.943-1G>A XP_011523696.1:p.=
XM_011525395.1:c.943-1G>A XP_011523697.1:p.=
XM_011525396.1:c.943-1G>A XP_011523698.1:p.=
XM_011525397.1:c.943-1G>A XP_011523699.1:p.=
XM_011525398.1:c.433-1G>A XP_011523700.1:p.=
XR_934581.1:n.1042-1G>A
XM_011525394.3:c.943-1G>A XP_011523696.1:p.=
XM_011525395.2:c.943-1G>A XP_011523697.1:p.=
XM_011525396.2:c.943-1G>A XP_011523698.1:p.=
XM_017025243.2:c.1261-1G>A XP_016880732.1:p.=
XM_017025244.2:c.943-1G>A XP_016880733.1:p.=
XR_001752670.2:n.1447-1G>A
XR_001752671.1:n.1054-1G>A
XR_001752672.1:n.1055-1G>A
XR_002958079.1:n.1053-1G>A
NM_003647.3:c.889-1G>A MANE Select NP_003638.1:p.=