LDH info

Canonical Allele Identifier: CA13091875
Gene: PTGS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10306122

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122373210T>C , CM000671.2:g.122373210T>C GRCh38
NC_000009.11:g.125135489T>C , CM000671.1:g.125135489T>C GRCh37
NC_000009.10:g.124175310T>C NCBI36
NG_032900.1:g.7261T>C

Transcript Alleles

HGVS Amino-acid change
NM_000962.3:c.94+1938T>C VV NP_000953.2:p.=
NM_001271164.1:c.94+1938T>C VV NP_001258093.1:p.=
NM_001271166.1:c.-234+1938T>C VV NP_001258095.1:p.=
NM_001271367.1:c.-205+1938T>C VV NP_001258296.1:p.=
NM_001271368.1:c.19+1376T>C VV NP_001258297.1:p.=
NM_080591.2:c.94+1938T>C VV NP_542158.1:p.=
XM_005252105.2:c.19+1376T>C XP_005252162.1:p.=
XM_011518875.1:c.19+1376T>C XP_011517177.1:p.=
XM_011518876.1:c.-2468T>C XP_011517178.1:p.=
XM_005252105.3:c.19+1376T>C XP_005252162.1:p.=
XM_011518875.2:c.19+1376T>C XP_011517177.1:p.=
XM_011518876.2:c.-2468T>C XP_011517178.1:p.=
XM_024447614.1:c.-234+1938T>C XP_024303382.1:p.=
XM_024447615.1:c.-234+1938T>C XP_024303383.1:p.=
NM_000962.4:c.94+1938T>C VV MANE Preferred NP_000953.2:p.=
NM_001271164.2:c.94+1938T>C VV NP_001258093.1:p.=
NM_001271166.2:c.-234+1938T>C VV NP_001258095.1:p.=
NM_001271367.2:c.-205+1938T>C VV NP_001258296.1:p.=
NM_001271368.2:c.19+1376T>C VV NP_001258297.1:p.=
NM_080591.3:c.94+1938T>C VV NP_542158.1:p.=
ENST00000223423.8:c.94+1938T>C ENSP00000223423.4:p.=
ENST00000362012.6:c.94+1938T>C ENSP00000354612.2:p.=
ENST00000426608.5:n.85+1938T>C ENSP00000411606.1:p.=
ENST00000540753.5:c.19+1376T>C ENSP00000437709.1:p.=
ENST00000614910.4:c.94+1938T>C ENSP00000484800.1:p.=
ENST00000619306.4:n.187+1938T>C ENSP00000483540.1:p.=