LDH info

Canonical Allele Identifier: CA342672
Gene: SLC22A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 25411
dbSNP Id: rs144547521

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390830C>T , CM000667.2:g.132390830C>T GRCh38
NC_000005.9:g.131726522C>T , CM000667.1:g.131726522C>T GRCh37
NC_000005.8:g.131754421C>T NCBI36
NG_008982.1:g.26122C>T
NG_008982.2:g.26127C>T

Transcript Alleles

HGVS Amino-acid change
NM_001308122.1:c.1265C>T VV NP_001295051.1:p.Pro422Leu
NM_003060.3:c.1193C>T VV NP_003051.1:p.Pro398Leu
XM_011543590.1:c.575C>T XP_011541892.1:p.Pro192Leu
XR_427718.1:n.1553C>T
XR_948290.1:n.1394-1603C>T
XR_948291.1:n.1547C>T
XM_011543590.2:c.575C>T XP_011541892.1:p.Pro192Leu
XM_017009778.2:c.665C>T XP_016865267.1:p.Pro222Leu
XR_001742215.1:n.1448C>T
XR_001742216.1:n.1467C>T
XR_427718.2:n.1553C>T
XR_948290.2:n.1394-1603C>T
XR_948291.2:n.1547C>T
ENST00000245407.7:c.1193C>T ENSP00000245407.3:p.Pro398Leu
ENST00000435065.6:n.1265C>T ENSP00000402760.2:p.Pro422Leu
ENST00000447841.5:n.112-1603C>T
ENST00000448810.5:n.455C>T
ENST00000461013.5:n.8615C>T
ENST00000475308.1:n.1871C>T
ENST00000479605.5:n.296C>T