LDH info

Canonical Allele Identifier: CA121757
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11898
ClinVar RCV Id: RCV000012673
dbSNP Id: rs28934608

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280333C>T , CM000666.2:g.186280333C>T GRCh38
NC_000004.11:g.187201487C>T , CM000666.1:g.187201487C>T GRCh37
NC_000004.10:g.187438481C>T NCBI36
NG_008051.1:g.19370C>T , LRG_583:g.19370C>T

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.976C>T , LRG_583t1:c.976C>T NP_000119.1:p.Arg326Cys
XM_005262821.2:c.976C>T XP_005262878.1:p.Arg326Cys
XM_005262822.2:c.976C>T XP_005262879.1:p.Arg326Cys
XM_005262823.2:c.706C>T XP_005262880.1:p.Arg236Cys
XM_005262824.1:c.976C>T XP_005262881.1:p.Arg326Cys
XM_006714137.1:c.928C>T XP_006714200.1:p.Arg310Cys
XR_938706.1:n.1328C>T
XR_938707.1:n.1328C>T
XM_005262821.4:c.976C>T XP_005262878.1:p.Arg326Cys
XM_005262822.4:c.976C>T XP_005262879.1:p.Arg326Cys
XM_005262823.4:c.706C>T XP_005262880.1:p.Arg236Cys
XM_006714137.3:c.928C>T XP_006714200.1:p.Arg310Cys
XM_017007884.2:c.976C>T XP_016863373.1:p.Arg326Cys
XM_017007885.2:c.976C>T XP_016863374.1:p.Arg326Cys
XM_017007886.2:c.976C>T XP_016863375.1:p.Arg326Cys
XR_001741172.2:n.1309C>T
NM_000128.4:c.976C>T VV MANE Preferred NP_000119.1:p.Arg326Cys
ENST00000264692.8:c.814C>T ENSP00000264692.5:p.Arg272Cys
ENST00000403665.6:c.976C>T ENSP00000384957.2:p.Arg326Cys
ENST00000452239.1:n.423C>T