Canonical Allele Identifier: CA2266995159

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848874_56848877delinsAAGT , CM000679.2:g.56848874_56848877delinsAAGT GRCh38
NC_000017.10:g.54926235_54926238delinsAAGT , CM000679.1:g.54926235_54926238delinsAAGT GRCh37
NC_000017.9:g.52281234_52281237delinsAAGT NCBI36
NG_033888.1:g.19776_19779delinsAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+21_1046+24delinsAAGT (DGKE) MANE Select ENSP00000284061.3:n.1046+21_1046+24delinsAAGT
ENST00000648772.1:c.*313+3066_*313+3069delinsACTT (TRIM25) ENSP00000498158.1:n.*313+3066_*313+3069delinsACTT
ENST00000284061.7:c.1046+21_1046+24delinsAAGT (DGKE) ENSP00000284061.3:n.1046+21_1046+24delinsAAGT
ENST00000572944.1:c.876+21_876+24delinsAAGT (DGKE)
NM_003647.2:c.1046+21_1046+24delinsAAGT (DGKE) NP_003638.1:n.1046+21_1046+24delinsAAGT
XM_011525394.1:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523696.1:n.1100+21_1100+24delinsAAGT
XM_011525395.1:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523697.1:n.1100+21_1100+24delinsAAGT
XM_011525396.1:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523698.1:n.1100+21_1100+24delinsAAGT
XM_011525397.1:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523699.1:n.1100+21_1100+24delinsAAGT
XM_011525398.1:c.590+21_590+24delinsAAGT (DGKE) XP_011523700.1:n.590+21_590+24delinsAAGT
XR_934581.1:n.1199+21_1199+24delinsAAGT (DGKE)
XM_011525394.3:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523696.1:n.1100+21_1100+24delinsAAGT
XM_011525395.2:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523697.1:n.1100+21_1100+24delinsAAGT
XM_011525396.2:c.1100+21_1100+24delinsAAGT (DGKE) XP_011523698.1:n.1100+21_1100+24delinsAAGT
XM_017025243.2:c.1418+21_1418+24delinsAAGT (DGKE) XP_016880732.1:n.1418+21_1418+24delinsAAGT
XM_017025244.2:c.1100+21_1100+24delinsAAGT (DGKE) XP_016880733.1:n.1100+21_1100+24delinsAAGT
XR_001752670.2:n.1604+21_1604+24delinsAAGT (DGKE)
XR_001752671.1:n.1211+21_1211+24delinsAAGT (DGKE)
XR_001752672.1:n.1212+21_1212+24delinsAAGT (DGKE)
XR_002958079.1:n.1210+21_1210+24delinsAAGT (DGKE)
NM_003647.3:c.1046+21_1046+24delinsAAGT (DGKE) MANE Select NP_003638.1:n.1046+21_1046+24delinsAAGT