LDH info

Canonical Allele Identifier: CA323959
Gene: PDHA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 214941
dbSNP Id: rs863224150

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19353169C>T , CM000685.2:g.19353169C>T GRCh38
NC_000023.10:g.19371287C>T , CM000685.1:g.19371287C>T GRCh37
NC_000023.9:g.19281208C>T NCBI36
NG_016781.1:g.14277C>T

Transcript Alleles

HGVS Amino-acid change
NM_000284.3:c.506C>T VV NP_000275.1:p.Ala169Val
NM_001173454.1:c.620C>T VV NP_001166925.1:p.Ala207Val
NM_001173455.1:c.527C>T VV NP_001166926.1:p.Ala176Val
NM_001173456.1:c.506C>T VV NP_001166927.1:p.Ala169Val
XM_011545531.1:c.641C>T XP_011543833.1:p.Ala214Val
XM_011545532.1:c.641C>T XP_011543834.1:p.Ala214Val
XM_017029574.2:c.620C>T XP_016885063.1:p.Ala207Val
NM_000284.4:c.506C>T VV MANE Preferred NP_000275.1:p.Ala169Val
ENST00000355808.9:c.527C>T ENSP00000348062.5:p.Ala176Val
ENST00000379805.3:c.506C>T ENSP00000369133.3:p.Ala169Val
ENST00000379806.9:c.620C>T ENSP00000369134.5:p.Ala207Val
ENST00000422285.6:c.506C>T ENSP00000394382.2:p.Ala169Val
ENST00000479146.1:n.341C>T
ENST00000540249.5:c.506C>T ENSP00000440761.1:p.Ala169Val
ENST00000545074.5:c.527C>T ENSP00000438550.1:p.Ala176Val