Canonical Allele Identifier: CA379508738
Gene: LDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407152T>G , CM000673.2:g.18407152T>G GRCh38
NC_000011.9:g.18428699T>G , CM000673.1:g.18428699T>G GRCh37
NC_000011.8:g.18385275T>G NCBI36
NG_008185.1:g.17718T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.870T>G MANE Select ENSP00000395337.3:p.Ser290Arg
ENST00000227157.8:c.*20T>G ENSP00000227157.4:n.*20T>G
ENST00000375710.7:n.1737T>G
ENST00000379412.9:c.870T>G ENSP00000368722.5:p.Ser290Arg
ENST00000396222.6:c.688-87T>G ENSP00000379524.2:n.688-87T>G
ENST00000422447.7:c.870T>G ENSP00000395337.3:p.Ser290Arg
ENST00000430553.6:c.696T>G ENSP00000406172.2:p.Ser232Arg
ENST00000538451.1:n.757T>G
ENST00000540430.5:c.957T>G ENSP00000445175.1:p.Ser319Arg
ENST00000541097.5:c.*208T>G ENSP00000443362.1:n.*208T>G
ENST00000542179.1:c.870T>G ENSP00000445331.1:p.Ser290Arg
ENST00000545215.5:c.*614T>G ENSP00000442637.1:n.*614T>G
NM_001135239.1:c.696T>G NP_001128711.1:p.Ser232Arg
NM_001165414.1:c.957T>G NP_001158886.1:p.Ser319Arg
NM_001165415.1:c.688-87T>G NP_001158887.1:n.688-87T>G
NM_001165416.1:c.*20T>G NP_001158888.1:n.*20T>G
NM_005566.3:c.870T>G NP_005557.1:p.Ser290Arg
NR_028500.1:n.1024T>G
NM_005566.4:c.870T>G MANE Select NP_005557.1:p.Ser290Arg
NM_001165415.2:c.688-87T>G NP_001158887.1:n.688-87T>G
NM_001135239.2:c.696T>G NP_001128711.1:p.Ser232Arg
NM_001165414.2:c.957T>G NP_001158886.1:p.Ser319Arg
NM_001165416.2:c.*20T>G NP_001158888.1:n.*20T>G
NR_028500.2:n.850T>G