LDH info

Canonical Allele Identifier: CA16355327
Gene: PTPRD HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7849581

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.9924724C>T , CM000671.2:g.9924724C>T GRCh38
NC_000009.11:g.9924724C>T , CM000671.1:g.9924724C>T GRCh37
NC_000009.10:g.9914724C>T NCBI36
NG_033963.1:g.693000G>A

Transcript Alleles

HGVS Amino-acid change
NM_002839.3:c.-368+13783G>A VV NP_002830.1:p.=
XM_011517980.1:c.-329+13783G>A XP_011516282.1:p.=
XM_011517992.1:c.-368+13783G>A XP_011516294.1:p.=
XM_006716817.4:c.-368+13783G>A XP_006716880.1:p.=
XM_006716823.3:c.-368+13783G>A XP_006716886.1:p.=
XM_006716825.4:c.-368+13783G>A XP_006716888.1:p.=
XM_006716827.4:c.-368+13783G>A XP_006716890.1:p.=
XM_006716832.4:c.-368+13783G>A XP_006716895.1:p.=
XM_006716833.4:c.-368+13783G>A XP_006716896.1:p.=
XM_006716834.4:c.-368+13783G>A XP_006716897.1:p.=
XM_006716835.4:c.-368+13783G>A XP_006716898.1:p.=
XM_006716837.4:c.-368+13783G>A XP_006716900.1:p.=
XM_011517992.3:c.-368+13783G>A XP_011516294.1:p.=
XM_017014958.2:c.-368+13783G>A XP_016870447.1:p.=
XM_017014959.2:c.-440+13783G>A XP_016870448.1:p.=
XM_017014960.2:c.-329+13783G>A XP_016870449.1:p.=
XM_017014961.2:c.-368+13783G>A XP_016870450.1:p.=
XM_017014963.2:c.-368+13783G>A XP_016870452.1:p.=
XM_017014964.2:c.-368+13783G>A XP_016870453.1:p.=
XM_017014965.2:c.-368+13783G>A XP_016870454.1:p.=
XM_017014966.2:c.-368+13783G>A XP_016870455.1:p.=
XM_017014967.2:c.-368+13783G>A XP_016870456.1:p.=
XM_017014968.2:c.-368+13783G>A XP_016870457.1:p.=
XM_017014969.2:c.-368+13783G>A XP_016870458.1:p.=
XM_017014970.2:c.-368+13783G>A XP_016870459.1:p.=
XM_017014971.2:c.-368+13783G>A XP_016870460.1:p.=
XM_017014972.2:c.-368+13783G>A XP_016870461.1:p.=
XM_017014973.2:c.-368+13783G>A XP_016870462.1:p.=
XM_017014974.2:c.-368+13783G>A XP_016870463.1:p.=
XM_017014975.2:c.-368+13783G>A XP_016870464.1:p.=
XM_017014976.2:c.-368+13783G>A XP_016870465.1:p.=
XM_017014977.2:c.-368+13783G>A XP_016870466.1:p.=
XM_017014978.2:c.-368+13783G>A XP_016870467.1:p.=
XM_017014979.2:c.-368+13783G>A XP_016870468.1:p.=
XM_017014980.2:c.-368+13783G>A XP_016870469.1:p.=
XM_017014981.2:c.-368+13783G>A XP_016870470.1:p.=
XM_017014982.2:c.-368+13783G>A XP_016870471.1:p.=
XM_017014983.2:c.-368+13783G>A XP_016870472.1:p.=
XM_017014984.2:c.-368+13783G>A XP_016870473.1:p.=
XM_017014985.2:c.-368+13783G>A XP_016870474.1:p.=
XM_017014986.2:c.-368+13783G>A XP_016870475.1:p.=
XM_017014987.2:c.-368+13783G>A XP_016870476.1:p.=
XM_017014988.2:c.-368+13783G>A XP_016870477.1:p.=
XM_017014989.2:c.-368+13783G>A XP_016870478.1:p.=
XM_017014990.2:c.-368+13783G>A XP_016870479.1:p.=
XM_017014991.2:c.-368+13783G>A XP_016870480.1:p.=
XM_017014992.2:c.-368+13783G>A XP_016870481.1:p.=
XM_017014993.2:c.-368+13783G>A XP_016870482.1:p.=
XM_017014994.2:c.-368+13783G>A XP_016870483.1:p.=
XM_017014995.2:c.-368+13783G>A XP_016870484.1:p.=
XM_024447625.1:c.-368+13783G>A XP_024303393.1:p.=
XM_024447627.1:c.-5819+13783G>A XP_024303395.1:p.=
NM_002839.4:c.-368+13783G>A VV NP_002830.1:p.=
ENST00000381196.8:c.-368+13783G>A ENSP00000370593.3:p.=
ENST00000463477.5:c.-440+13783G>A ENSP00000417661.1:p.=