Canonical Allele Identifier: CA984903541

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1907484374
• gnomAD v3: 17-56848991-GTGTTT-G
• gnomAD v4: 17-56848991-GTGTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848998_56849002del , CM000679.2:g.56848998_56849002del	GRCh38
NC_000017.10:g.54926359_54926363del , CM000679.1:g.54926359_54926363del	GRCh37
NC_000017.9:g.52281358_52281362del	NCBI36
NG_033888.1:g.19900_19904del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+145_1046+149del (DGKE) MANE Select	ENSP00000284061.3:n.1046+145_1046+149del
ENST00000648772.1:c.*313+2947_*313+2951del (TRIM25)	ENSP00000498158.1:n.*313+2947_*313+2951del
ENST00000284061.7:c.1046+145_1046+149del (DGKE)	ENSP00000284061.3:n.1046+145_1046+149del
ENST00000572944.1:c.876+145_876+149del (DGKE)
NM_003647.2:c.1046+145_1046+149del (DGKE)	NP_003638.1:n.1046+145_1046+149del
XM_011525394.1:c.1100+145_1100+149del (DGKE)	XP_011523696.1:n.1100+145_1100+149del
XM_011525395.1:c.1100+145_1100+149del (DGKE)	XP_011523697.1:n.1100+145_1100+149del
XM_011525396.1:c.1100+145_1100+149del (DGKE)	XP_011523698.1:n.1100+145_1100+149del
XM_011525397.1:c.1100+145_1100+149del (DGKE)	XP_011523699.1:n.1100+145_1100+149del
XM_011525398.1:c.590+145_590+149del (DGKE)	XP_011523700.1:n.590+145_590+149del
XR_934581.1:n.1199+145_1199+149del (DGKE)
XM_011525394.3:c.1100+145_1100+149del (DGKE)	XP_011523696.1:n.1100+145_1100+149del
XM_011525395.2:c.1100+145_1100+149del (DGKE)	XP_011523697.1:n.1100+145_1100+149del
XM_011525396.2:c.1100+145_1100+149del (DGKE)	XP_011523698.1:n.1100+145_1100+149del
XM_017025243.2:c.1418+145_1418+149del (DGKE)	XP_016880732.1:n.1418+145_1418+149del
XM_017025244.2:c.1100+145_1100+149del (DGKE)	XP_016880733.1:n.1100+145_1100+149del
XR_001752670.2:n.1604+145_1604+149del (DGKE)
XR_001752671.1:n.1211+145_1211+149del (DGKE)
XR_001752672.1:n.1212+145_1212+149del (DGKE)
XR_002958079.1:n.1210+145_1210+149del (DGKE)
NM_003647.3:c.1046+145_1046+149del (DGKE) MANE Select	NP_003638.1:n.1046+145_1046+149del