Canonical Allele Identifier: CA626780145

Linked Data

dbSNP Id: rs1396771317

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848887_56848888insTCCCT , CM000679.2:g.56848887_56848888insTCCCT GRCh38
NC_000017.10:g.54926248_54926249insTCCCT , CM000679.1:g.54926248_54926249insTCCCT GRCh37
NC_000017.9:g.52281247_52281248insTCCCT NCBI36
NG_033888.1:g.19789_19790insTCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+34_1046+35insTCCCT (DGKE) MANE Select ENSP00000284061.3:n.1046+34_1046+35insTCCCT
ENST00000648772.1:c.*313+3055_*313+3056insAGGGA (TRIM25) ENSP00000498158.1:n.*313+3055_*313+3056insAGGGA
ENST00000284061.7:c.1046+34_1046+35insTCCCT (DGKE) ENSP00000284061.3:n.1046+34_1046+35insTCCCT
ENST00000572944.1:c.876+34_876+35insTCCCT (DGKE)
NM_003647.2:c.1046+34_1046+35insTCCCT (DGKE) NP_003638.1:n.1046+34_1046+35insTCCCT
XM_011525394.1:c.1100+34_1100+35insTCCCT (DGKE) XP_011523696.1:n.1100+34_1100+35insTCCCT
XM_011525395.1:c.1100+34_1100+35insTCCCT (DGKE) XP_011523697.1:n.1100+34_1100+35insTCCCT
XM_011525396.1:c.1100+34_1100+35insTCCCT (DGKE) XP_011523698.1:n.1100+34_1100+35insTCCCT
XM_011525397.1:c.1100+34_1100+35insTCCCT (DGKE) XP_011523699.1:n.1100+34_1100+35insTCCCT
XM_011525398.1:c.590+34_590+35insTCCCT (DGKE) XP_011523700.1:n.590+34_590+35insTCCCT
XR_934581.1:n.1199+34_1199+35insTCCCT (DGKE)
XM_011525394.3:c.1100+34_1100+35insTCCCT (DGKE) XP_011523696.1:n.1100+34_1100+35insTCCCT
XM_011525395.2:c.1100+34_1100+35insTCCCT (DGKE) XP_011523697.1:n.1100+34_1100+35insTCCCT
XM_011525396.2:c.1100+34_1100+35insTCCCT (DGKE) XP_011523698.1:n.1100+34_1100+35insTCCCT
XM_017025243.2:c.1418+34_1418+35insTCCCT (DGKE) XP_016880732.1:n.1418+34_1418+35insTCCCT
XM_017025244.2:c.1100+34_1100+35insTCCCT (DGKE) XP_016880733.1:n.1100+34_1100+35insTCCCT
XR_001752670.2:n.1604+34_1604+35insTCCCT (DGKE)
XR_001752671.1:n.1211+34_1211+35insTCCCT (DGKE)
XR_001752672.1:n.1212+34_1212+35insTCCCT (DGKE)
XR_002958079.1:n.1210+34_1210+35insTCCCT (DGKE)
NM_003647.3:c.1046+34_1046+35insTCCCT (DGKE) MANE Select NP_003638.1:n.1046+34_1046+35insTCCCT