Canonical Allele Identifier: CA2638886962

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848960_56848961insTACAACTAGTATAGTCTTTC , CM000679.2:g.56848960_56848961insTACAACTAGTATAGTCTTTC GRCh38
NC_000017.10:g.54926321_54926322insTACAACTAGTATAGTCTTTC , CM000679.1:g.54926321_54926322insTACAACTAGTATAGTCTTTC GRCh37
NC_000017.9:g.52281320_52281321insTACAACTAGTATAGTCTTTC NCBI36
NG_033888.1:g.19862_19863insTACAACTAGTATAGTCTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+107_1046+108insTACAACTAGTATAGTCTTTC (DGKE) MANE Select ENSP00000284061.3:n.1046+107_1046+108insTACAACTAGTATAGTCTTTC
ENST00000648772.1:c.*313+2982_*313+2983insGAAAGACTATACTAGTTGTA (TRIM25) ENSP00000498158.1:n.*313+2982_*313+2983insGAAAGACTATACTAGTTGT...
ENST00000284061.7:c.1046+107_1046+108insTACAACTAGTATAGTCTTTC (DGKE) ENSP00000284061.3:n.1046+107_1046+108insTACAACTAGTATAGTCTTTC
ENST00000572944.1:c.876+107_876+108insTACAACTAGTATAGTCTTTC (DGKE)
NM_003647.2:c.1046+107_1046+108insTACAACTAGTATAGTCTTTC (DGKE) NP_003638.1:n.1046+107_1046+108insTACAACTAGTATAGTCTTTC
XM_011525394.1:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523696.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525395.1:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523697.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525396.1:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523698.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525397.1:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523699.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525398.1:c.590+107_590+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523700.1:n.590+107_590+108insTACAACTAGTATAGTCTTTC
XR_934581.1:n.1199+107_1199+108insTACAACTAGTATAGTCTTTC (DGKE)
XM_011525394.3:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523696.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525395.2:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523697.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_011525396.2:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_011523698.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XM_017025243.2:c.1418+107_1418+108insTACAACTAGTATAGTCTTTC (DGKE) XP_016880732.1:n.1418+107_1418+108insTACAACTAGTATAGTCTTTC
XM_017025244.2:c.1100+107_1100+108insTACAACTAGTATAGTCTTTC (DGKE) XP_016880733.1:n.1100+107_1100+108insTACAACTAGTATAGTCTTTC
XR_001752670.2:n.1604+107_1604+108insTACAACTAGTATAGTCTTTC (DGKE)
XR_001752671.1:n.1211+107_1211+108insTACAACTAGTATAGTCTTTC (DGKE)
XR_001752672.1:n.1212+107_1212+108insTACAACTAGTATAGTCTTTC (DGKE)
XR_002958079.1:n.1210+107_1210+108insTACAACTAGTATAGTCTTTC (DGKE)
NM_003647.3:c.1046+107_1046+108insTACAACTAGTATAGTCTTTC (DGKE) MANE Select NP_003638.1:n.1046+107_1046+108insTACAACTAGTATAGTCTTTC