LDH info

Canonical Allele Identifier: CA557396098
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 558063
ClinVar RCV Id: RCV000674279
dbSNP Id: rs1459304265

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276276_186276281del , CM000666.2:g.186276276_186276281del GRCh38
NC_000004.11:g.187197430_187197435del , CM000666.1:g.187197430_187197435del GRCh37
NC_000004.10:g.187434424_187434429del NCBI36
NG_008051.1:g.15313_15318del , LRG_583:g.15313_15318del

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.641_646del , LRG_583t1:c.641_646del NP_000119.1:p.Ile215_Asp216del
XM_005262821.2:c.641_646del XP_005262878.1:p.Ile215_Asp216del
XM_005262822.2:c.641_646del XP_005262879.1:p.Ile215_Asp216del
XM_005262823.2:c.485+2001_485+2006del XP_005262880.1:p.=
XM_005262824.1:c.641_646del XP_005262881.1:p.Ile215_Asp216del
XM_006714137.1:c.641_646del XP_006714200.1:p.Ile215_Asp216del
XR_938706.1:n.993_998del
XR_938707.1:n.993_998del
XM_005262821.4:c.641_646del XP_005262878.1:p.Ile215_Asp216del
XM_005262822.4:c.641_646del XP_005262879.1:p.Ile215_Asp216del
XM_005262823.4:c.485+2001_485+2006del XP_005262880.1:p.=
XM_006714137.3:c.641_646del XP_006714200.1:p.Ile215_Asp216del
XM_017007884.2:c.641_646del XP_016863373.1:p.Ile215_Asp216del
XM_017007885.2:c.641_646del XP_016863374.1:p.Ile215_Asp216del
XM_017007886.2:c.641_646del XP_016863375.1:p.Ile215_Asp216del
XR_001741172.2:n.974_979del
NM_000128.4:c.641_646del VV MANE Preferred NP_000119.1:p.Ile215_Asp216del
ENST00000264692.8:c.479_484del ENSP00000264692.5:p.Ile161_Asp162del
ENST00000403665.6:c.641_646del ENSP00000384957.2:p.Ile215_Asp216del
ENST00000452239.1:n.88_93del