LDH info

Canonical Allele Identifier: CA10576196
Gene: C11orf65 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225942
ClinVar RCV Id: RCV000211248
dbSNP Id: rs11212617

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108412434C>A , CM000673.2:g.108412434C>A GRCh38
NC_000011.9:g.108283161C>A , CM000673.1:g.108283161C>A GRCh37
NC_000011.8:g.107788371C>A NCBI36
NG_054724.1:g.62399G>T

Transcript Alleles

HGVS Amino-acid change
NM_152587.3:c.175-5285G>T VV NP_689800.3:p.=
XM_005271412.2:c.175-5471G>T XP_005271469.1:p.=
XM_005271413.2:c.82-5285G>T XP_005271470.1:p.=
XM_005271414.3:c.175-5285G>T XP_005271471.1:p.=
XM_005271415.3:c.175-5285G>T XP_005271472.1:p.=
XM_011542639.1:c.175-5285G>T XP_011540941.1:p.=
XM_011542640.1:c.175-5285G>T XP_011540942.1:p.=
XM_011542641.1:c.82-5471G>T XP_011540943.1:p.=
XM_011542642.1:c.175-5285G>T XP_011540944.1:p.=
XM_011542643.1:c.175-5285G>T XP_011540945.1:p.=
NM_001330368.1:c.82-5471G>T VV NP_001317297.1:p.=
NM_001351110.1:c.82-5285G>T VV NP_001338039.1:p.=
NM_152587.4:c.175-5285G>T VV NP_689800.3:p.=
NR_147053.2:n.338-5285G>T
XM_005271412.3:c.175-5471G>T XP_005271469.1:p.=
XM_005271413.3:c.82-5285G>T XP_005271470.1:p.=
XM_005271414.4:c.175-5285G>T XP_005271471.1:p.=
XM_005271415.4:c.175-5285G>T XP_005271472.1:p.=
XM_011542639.2:c.175-5285G>T XP_011540941.1:p.=
XM_011542640.2:c.175-5285G>T XP_011540942.1:p.=
XM_011542641.2:c.82-5471G>T XP_011540943.1:p.=
XM_011542643.2:c.175-5285G>T XP_011540945.1:p.=
XM_017017246.1:c.175-5285G>T XP_016872735.1:p.=
XM_017017247.1:c.175-5285G>T XP_016872736.1:p.=
XM_017017248.1:c.175-5285G>T XP_016872737.1:p.=
NM_152587.5:c.175-5285G>T VV MANE Preferred NP_689800.3:p.=
NM_001330368.2:c.82-5471G>T VV NP_001317297.1:p.=
NM_001351110.2:c.82-5285G>T VV NP_001338039.1:p.=
NR_147053.3:n.336-5285G>T
ENST00000393084.5:c.175-5285G>T ENSP00000376799.1:p.=
ENST00000525729.5:c.82-5471G>T ENSP00000433395.1:p.=
ENST00000527531.5:c.175-5285G>T ENSP00000431706.1:p.=
ENST00000529391.5:c.175-5285G>T ENSP00000436400.1:p.=
ENST00000533583.1:c.175-5471G>T ENSP00000434500.1:p.=
ENST00000615746.4:c.175-5285G>T ENSP00000483537.1:p.=