LDH info

Canonical Allele Identifier: CA342150
Gene: SLC25A13 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21509
ClinVar RCV Id: RCV000020699
dbSNP Id: rs80338724

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121997C>T , CM000669.2:g.96121997C>T GRCh38
NC_000007.13:g.95751309C>T , CM000669.1:g.95751309C>T GRCh37
NC_000007.12:g.95589245C>T NCBI36
NG_012247.1:g.205151G>A
NG_012247.2:g.205151G>A

Transcript Alleles

HGVS Amino-acid change
NM_001160210.1:c.1595G>A VV NP_001153682.1:p.Gly532Asp
NM_014251.2:c.1592G>A VV NP_055066.1:p.Gly531Asp
NR_027662.1:n.1667G>A
XM_006715831.2:c.1625G>A XP_006715894.1:p.Gly542Asp
XM_011515728.1:c.740G>A XP_011514030.1:p.Gly247Asp
XM_006715831.4:c.1625G>A XP_006715894.1:p.Gly542Asp
XM_017011663.1:c.1583G>A XP_016867152.1:p.Gly528Asp
XM_017011664.2:c.740G>A XP_016867153.1:p.Gly247Asp
XM_017011665.1:c.740G>A XP_016867154.1:p.Gly247Asp
XR_001744525.2:n.1838G>A
XR_002956405.1:n.2396G>A
ENST00000265631.9:c.1592G>A ENSP00000265631.5:p.Gly531Asp
ENST00000416240.6:c.1595G>A ENSP00000400101.2:p.Gly532Asp
ENST00000494085.1:n.2G>A