LDH info

Canonical Allele Identifier: CA114384
Gene: PROC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 656
ClinVar RCV Id: RCV000000690
dbSNP Id: rs121918141

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428602C>T , CM000664.2:g.127428602C>T GRCh38
NC_000002.11:g.128186178C>T , CM000664.1:g.128186178C>T GRCh37
NC_000002.10:g.127902648C>T NCBI36
NG_016323.1:g.15183C>T , LRG_599:g.15183C>T

Transcript Alleles

HGVS Amino-acid change
NM_000312.3:c.1042C>T , LRG_599t1:c.1042C>T NP_000303.1:p.Arg348Ter
XM_005263715.3:c.1225C>T XP_005263772.1:p.Arg409Ter
XM_005263716.3:c.1207C>T XP_005263773.1:p.Arg403Ter
XM_005263717.3:c.1105C>T XP_005263774.1:p.Arg369Ter
XR_923313.1:n.1332-338G>A
XM_005263717.4:c.1105C>T XP_005263774.1:p.Arg369Ter
XM_017004505.1:c.1285C>T XP_016859994.1:p.Arg429Ter
XM_024453002.1:c.1387C>T XP_024308770.1:p.Arg463Ter
XM_024453003.1:c.1327C>T XP_024308771.1:p.Arg443Ter
XM_024453004.1:c.1225C>T XP_024308772.1:p.Arg409Ter
XM_024453005.1:c.1207C>T XP_024308773.1:p.Arg403Ter
XM_024453006.1:c.1144C>T XP_024308774.1:p.Arg382Ter
XR_001739705.1:n.3607-338G>A
XR_923313.2:n.4043-338G>A
NM_000312.4:c.1042C>T VV MANE Preferred NP_000303.1:p.Arg348Ter
NM_001375602.1:c.1225C>T VV NP_001362531.1:p.Arg409Ter
NM_001375603.1:c.1207C>T VV NP_001362532.1:p.Arg403Ter
NM_001375604.1:c.1105C>T VV NP_001362533.1:p.Arg369Ter
NM_001375605.1:c.1144C>T VV NP_001362534.1:p.Arg382Ter
NM_001375606.1:c.1210C>T VV NP_001362535.1:p.Arg404Ter
NM_001375607.1:c.1228C>T VV NP_001362536.1:p.Arg410Ter
NM_001375608.1:c.985C>T VV NP_001362537.1:p.Arg329Ter
NM_001375609.1:c.1018C>T VV NP_001362538.1:p.Arg340Ter
NM_001375610.1:c.1036C>T VV NP_001362539.1:p.Arg346Ter
NM_001375611.1:c.1042C>T VV NP_001362540.1:p.Arg348Ter
NM_001375613.1:c.1042C>T VV NP_001362542.1:p.Arg348Ter
ENST00000234071.7:c.1042C>T ENSP00000234071.3:p.Arg348Ter
ENST00000402125.2:n.366C>T
ENST00000409048.1:c.1144C>T ENSP00000386679.1:p.Arg382Ter