LDH info

Canonical Allele Identifier: CA11351507
Gene: PPARG HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1175540

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12423744C>A , CM000665.2:g.12423744C>A GRCh38
NC_000003.11:g.12465243C>A , CM000665.1:g.12465243C>A GRCh37
NC_000003.10:g.12440243C>A NCBI36
NG_011749.1:g.140895C>A

Transcript Alleles

HGVS Amino-acid change
NM_005037.5:c.1186+6590C>A VV NP_005028.4:p.=
NM_015869.4:c.1270+6590C>A VV NP_056953.2:p.=
NM_138711.3:c.1186+6590C>A VV NP_619725.2:p.=
NM_138712.3:c.1186+6590C>A VV NP_619726.2:p.=
XM_011533840.1:c.1186+6590C>A XP_011532142.1:p.=
XM_011533841.1:c.1186+6590C>A XP_011532143.1:p.=
XM_011533842.1:c.1270+6590C>A XP_011532144.1:p.=
XM_011533843.1:c.820-10154C>A XP_011532145.1:p.=
XM_011533844.1:c.736-10154C>A XP_011532146.1:p.=
NM_001330615.1:c.736-10154C>A VV NP_001317544.1:p.=
NM_001354666.1:c.1186+6590C>A VV NP_001341595.1:p.=
NM_001354667.1:c.1186+6590C>A VV NP_001341596.1:p.=
NM_001354669.1:c.553+6590C>A VV NP_001341598.1:p.=
XM_011533842.2:c.1270+6590C>A XP_011532144.1:p.=
XM_011533843.2:c.820-10154C>A XP_011532145.1:p.=
XM_024453604.1:c.1186+6590C>A XP_024309372.1:p.=
XM_024453605.1:c.1186+6590C>A XP_024309373.1:p.=
XM_024453606.1:c.1186+6590C>A XP_024309374.1:p.=
ENST00000287820.10:c.1270+6590C>A ENSP00000287820.6:p.=
ENST00000309576.10:c.1186+6590C>A ENSP00000312472.6:p.=
ENST00000397000.5:c.736-10154C>A ENSP00000380196.1:p.=
ENST00000397010.6:c.1186+6590C>A ENSP00000380205.2:p.=
ENST00000397012.6:c.1186+6590C>A ENSP00000380207.2:p.=
ENST00000397015.6:c.1186+6590C>A ENSP00000380210.2:p.=
ENST00000397023.5:c.*1408+6590C>A ENSP00000380218.1:p.=
ENST00000397026.6:c.1204+6590C>A ENSP00000380221.2:p.=