LDH info

Canonical Allele Identifier: CA16040941
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371284
ClinVar RCV Id: RCV000409581
dbSNP Id: rs1057517151

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186273141del , CM000666.2:g.186273141del GRCh38
NC_000004.11:g.187194295del , CM000666.1:g.187194295del GRCh37
NC_000004.10:g.187431289del NCBI36
NG_008051.1:g.12178del , LRG_583:g.12178del

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.289del , LRG_583t1:c.289del NP_000119.1:p.Tyr98IlefsTer10
XM_005262821.2:c.289del XP_005262878.1:p.Tyr98IlefsTer10
XM_005262822.2:c.289del XP_005262879.1:p.Tyr98IlefsTer10
XM_005262823.2:c.289del XP_005262880.1:p.Tyr98IlefsTer10
XM_005262824.1:c.289del XP_005262881.1:p.Tyr98IlefsTer10
XM_006714137.1:c.289del XP_006714200.1:p.Tyr98IlefsTer10
XR_938706.1:n.641del
XR_938707.1:n.641del
NM_001354804.1:c.289del VV NP_001341733.1:p.Tyr98IlefsTer10
XM_005262821.4:c.289del XP_005262878.1:p.Tyr98IlefsTer10
XM_005262822.4:c.289del XP_005262879.1:p.Tyr98IlefsTer10
XM_005262823.4:c.289del XP_005262880.1:p.Tyr98IlefsTer10
XM_006714137.3:c.289del XP_006714200.1:p.Tyr98IlefsTer10
XM_017007884.2:c.289del XP_016863373.1:p.Tyr98IlefsTer10
XM_017007885.2:c.289del XP_016863374.1:p.Tyr98IlefsTer10
XM_017007886.2:c.289del XP_016863375.1:p.Tyr98IlefsTer10
XR_001741172.2:n.622del
NM_000128.4:c.289del VV MANE Preferred NP_000119.1:p.Tyr98IlefsTer10
NM_001354804.2:c.289del VV NP_001341733.1:p.Tyr98IlefsTer10
ENST00000264692.8:c.289del ENSP00000264692.5:p.Tyr98IlefsTer10
ENST00000403665.6:c.289del ENSP00000384957.2:p.Tyr98IlefsTer10
ENST00000492972.6:c.289del ENSP00000424479.1:p.Tyr98IlefsTer10
ENST00000514715.1:n.161del