LDH info

Canonical Allele Identifier: CA5224636
Gene: PTGS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3842787

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122371228C>T , CM000671.2:g.122371228C>T GRCh38
NC_000009.11:g.125133507C>T , CM000671.1:g.125133507C>T GRCh37
NC_000009.10:g.124173328C>T NCBI36
NG_032900.1:g.5279C>T

Transcript Alleles

HGVS Amino-acid change
NM_000962.3:c.50C>T VV NP_000953.2:p.Pro17Leu
NM_001271164.1:c.50C>T VV NP_001258093.1:p.Pro17Leu
NM_001271166.1:c.-278C>T VV NP_001258095.1:p.=
NM_001271367.1:c.-249C>T VV NP_001258296.1:p.=
NM_001271368.1:c.-248C>T VV NP_001258297.1:p.=
NM_080591.2:c.50C>T VV NP_542158.1:p.Pro17Leu
XM_005252105.2:c.-248C>T XP_005252162.1:p.=
XM_011518875.1:c.-248C>T XP_011517177.1:p.=
XM_011518876.1:c.-4110C>T XP_011517178.1:p.=
XM_005252105.3:c.-248C>T XP_005252162.1:p.=
XM_011518875.2:c.-248C>T XP_011517177.1:p.=
XM_011518876.2:c.-4110C>T XP_011517178.1:p.=
XM_024447614.1:c.-278C>T XP_024303382.1:p.=
XM_024447615.1:c.-278C>T XP_024303383.1:p.=
NM_000962.4:c.50C>T VV MANE Preferred NP_000953.2:p.Pro17Leu
NM_001271164.2:c.50C>T VV NP_001258093.1:p.Pro17Leu
NM_001271166.2:c.-278C>T VV NP_001258095.1:p.=
NM_001271367.2:c.-249C>T VV NP_001258296.1:p.=
NM_001271368.2:c.-248C>T VV NP_001258297.1:p.=
NM_080591.3:c.50C>T VV NP_542158.1:p.Pro17Leu
ENST00000223423.8:c.50C>T ENSP00000223423.4:p.Pro17Leu
ENST00000362012.6:c.50C>T ENSP00000354612.2:p.Pro17Leu
ENST00000426608.5:n.41C>T ENSP00000411606.1:p.Pro14Leu
ENST00000540753.5:c.-248C>T ENSP00000437709.1:p.=
ENST00000614910.4:c.50C>T ENSP00000484800.1:p.Pro17Leu
ENST00000619306.4:n.143C>T ENSP00000483540.1:p.Pro48Leu