Canonical Allele Identifier: CA379509243
Gene: LDHA HGNC NCBI

Linked Data

dbSNP Id: rs1366763139

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407254G>A , CM000673.2:g.18407254G>A GRCh38
NC_000011.9:g.18428801G>A , CM000673.1:g.18428801G>A GRCh37
NC_000011.8:g.18385377G>A NCBI36
NG_008185.1:g.17820G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.972G>A MANE Select ENSP00000395337.3:p.Trp324Ter
ENST00000227157.8:c.*122G>A ENSP00000227157.4:n.*122G>A
ENST00000375710.7:n.1839G>A
ENST00000379412.9:c.972G>A ENSP00000368722.5:p.Trp324Ter
ENST00000396222.6:c.703G>A ENSP00000379524.2:p.Gly235Arg
ENST00000422447.7:c.972G>A ENSP00000395337.3:p.Trp324Ter
ENST00000430553.6:c.798G>A ENSP00000406172.2:p.Trp266Ter
ENST00000538451.1:n.859G>A
ENST00000540430.5:c.1059G>A ENSP00000445175.1:p.Trp353Ter
ENST00000542179.1:c.972G>A ENSP00000445331.1:p.Trp324Ter
ENST00000545215.5:c.*716G>A ENSP00000442637.1:n.*716G>A
NM_001135239.1:c.798G>A NP_001128711.1:p.Trp266Ter
NM_001165414.1:c.1059G>A NP_001158886.1:p.Trp353Ter
NM_001165415.1:c.703G>A NP_001158887.1:p.Gly235Arg
NM_001165416.1:c.*122G>A NP_001158888.1:n.*122G>A
NM_005566.3:c.972G>A NP_005557.1:p.Trp324Ter
NR_028500.1:n.1126G>A
NM_005566.4:c.972G>A MANE Select NP_005557.1:p.Trp324Ter
NM_001165415.2:c.703G>A NP_001158887.1:p.Gly235Arg
NM_001135239.2:c.798G>A NP_001128711.1:p.Trp266Ter
NM_001165414.2:c.1059G>A NP_001158886.1:p.Trp353Ter
NM_001165416.2:c.*122G>A NP_001158888.1:n.*122G>A
NR_028500.2:n.952G>A