Canonical Allele Identifier: CA5911454
Gene: LDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 391029
ClinVar RCV Id: RCV001704538
dbSNP Id: rs200383424

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407296A>G , CM000673.2:g.18407296A>G GRCh38
NC_000011.9:g.18428843A>G , CM000673.1:g.18428843A>G GRCh37
NC_000011.8:g.18385419A>G NCBI36
NG_008185.1:g.17862A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*15A>G MANE Select ENSP00000395337.3:n.*15A>G
ENST00000227157.8:c.*164A>G ENSP00000227157.4:n.*164A>G
ENST00000375710.7:n.1881A>G
ENST00000379412.9:c.*15A>G ENSP00000368722.5:n.*15A>G
ENST00000396222.6:c.745A>G ENSP00000379524.2:p.Ile249Val
ENST00000422447.7:c.*15A>G ENSP00000395337.3:n.*15A>G
ENST00000430553.6:c.*15A>G ENSP00000406172.2:n.*15A>G
ENST00000538451.1:n.901A>G
ENST00000540430.5:c.*15A>G ENSP00000445175.1:n.*15A>G
ENST00000545215.5:c.*758A>G ENSP00000442637.1:n.*758A>G
NM_001135239.1:c.*15A>G NP_001128711.1:n.*15A>G
NM_001165414.1:c.*15A>G NP_001158886.1:n.*15A>G
NM_001165415.1:c.745A>G NP_001158887.1:p.Ile249Val
NM_001165416.1:c.*164A>G NP_001158888.1:n.*164A>G
NM_005566.3:c.*15A>G NP_005557.1:n.*15A>G
NR_028500.1:n.1168A>G
NM_005566.4:c.*15A>G MANE Select NP_005557.1:n.*15A>G
NM_001165415.2:c.745A>G NP_001158887.1:p.Ile249Val
NM_001135239.2:c.*15A>G NP_001128711.1:n.*15A>G
NM_001165414.2:c.*15A>G NP_001158886.1:n.*15A>G
NM_001165416.2:c.*164A>G NP_001158888.1:n.*164A>G
NR_028500.2:n.994A>G