LDH info

Canonical Allele Identifier: CA5871731
Gene: RIC3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1528133

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8128206T>G , CM000673.2:g.8128206T>G GRCh38
NC_000011.9:g.8149753T>G , CM000673.1:g.8149753T>G GRCh37
NC_000011.8:g.8106329T>G NCBI36
NG_030416.1:g.45838A>C
NG_030416.2:g.45838A>C

Transcript Alleles

HGVS Amino-acid change
NM_001135109.2:c.125-17069A>C VV NP_001128581.1:p.=
NM_001206671.2:c.522-1399A>C VV NP_001193600.1:p.=
NM_001206672.2:c.427+10066A>C VV NP_001193601.1:p.=
NM_024557.4:c.522-1402A>C VV NP_078833.3:p.=
NR_045405.1:n.625-1399A>C
XM_006718317.2:c.522-1315A>C XP_006718380.1:p.=
XM_006718318.2:c.522-1402A>C XP_006718381.1:p.=
XR_428848.2:n.616-1315A>C
XR_428851.2:n.616-1315A>C
XR_930896.1:n.616-1315A>C
XR_930897.1:n.616-1315A>C
XR_930898.1:n.616-1315A>C
XR_930899.1:n.616-1315A>C
XR_930900.1:n.616-1315A>C
XR_930901.1:n.616-1399A>C
XR_930902.1:n.616-1402A>C
XR_930903.1:n.617-1399A>C
XR_930904.1:n.674+13A>C
XR_930905.1:n.737+13A>C
XR_930906.1:n.751+13A>C
NM_001135109.3:c.125-17069A>C VV NP_001128581.1:p.=
NM_001206671.3:c.522-1399A>C VV NP_001193600.1:p.=
NM_001206672.3:c.427+10066A>C VV NP_001193601.1:p.=
NM_001346690.1:c.38+13A>C VV NP_001333619.1:p.=
NM_001346691.1:c.521+9172A>C VV NP_001333620.1:p.=
NM_001346692.1:c.375-1402A>C VV NP_001333621.1:p.=
NM_001346693.1:c.375-1315A>C VV NP_001333622.1:p.=
NM_001346694.1:c.375-1399A>C VV NP_001333623.1:p.=
NM_024557.5:c.522-1402A>C VV NP_078833.3:p.=
NR_144484.1:n.533-1402A>C
NR_144485.1:n.676-1402A>C
NR_144497.1:n.230-1402A>C
XM_006718317.4:c.522-1315A>C XP_006718380.1:p.=
XM_006718318.4:c.522-1402A>C XP_006718381.1:p.=
XM_017018287.2:c.522-1315A>C XP_016873776.1:p.=
XM_024448684.1:c.375-1402A>C XP_024304452.1:p.=
XM_024448685.1:c.*39+13A>C XP_024304453.1:p.=
XM_024448686.1:c.*39+13A>C XP_024304454.1:p.=
XR_001747957.2:n.554-1402A>C
XR_001747959.2:n.2294+13A>C
XR_002957192.1:n.554-1402A>C
XR_002957193.1:n.554-1402A>C
XR_002957194.1:n.622-1315A>C
XR_002957195.1:n.553+9172A>C
XR_428848.4:n.554-1315A>C
XR_428851.4:n.554-1315A>C
XR_930896.3:n.554-1315A>C
XR_930897.3:n.554-1315A>C
XR_930898.3:n.554-1315A>C
XR_930900.3:n.554-1315A>C
XR_930901.3:n.554-1399A>C
XR_930903.3:n.622-1399A>C
XR_930904.3:n.2294+13A>C
XR_930905.3:n.2357+13A>C
NM_001206671.4:c.522-1399A>C VV MANE Preferred NP_001193600.1:p.=
ENST00000309737.10:n.522-1399A>C ENSP00000308820.6:p.=
ENST00000335425.7:c.125-17069A>C ENSP00000333988.7:p.=
ENST00000343202.8:c.522-1402A>C ENSP00000344904.4:p.=
ENST00000425599.6:n.427+10066A>C ENSP00000395320.2:p.=
ENST00000524799.5:n.383-1402A>C
ENST00000526962.1:c.125-1402A>C ENSP00000434787.1:p.=
ENST00000528463.5:c.*439-1399A>C ENSP00000435244.1:p.=
ENST00000530060.5:n.737+13A>C
ENST00000531450.1:c.522-1315A>C ENSP00000431658.1:p.=