Canonical Allele Identifier: CA379509530
Gene: LDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407285C>G , CM000673.2:g.18407285C>G GRCh38
NC_000011.9:g.18428832C>G , CM000673.1:g.18428832C>G GRCh37
NC_000011.8:g.18385408C>G NCBI36
NG_008185.1:g.17851C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*4C>G MANE Select ENSP00000395337.3:n.*4C>G
ENST00000227157.8:c.*153C>G ENSP00000227157.4:n.*153C>G
ENST00000375710.7:n.1870C>G
ENST00000379412.9:c.*4C>G ENSP00000368722.5:n.*4C>G
ENST00000396222.6:c.734C>G ENSP00000379524.2:p.Ser245Cys
ENST00000422447.7:c.*4C>G ENSP00000395337.3:n.*4C>G
ENST00000430553.6:c.*4C>G ENSP00000406172.2:n.*4C>G
ENST00000538451.1:n.890C>G
ENST00000540430.5:c.*4C>G ENSP00000445175.1:n.*4C>G
ENST00000545215.5:c.*747C>G ENSP00000442637.1:n.*747C>G
NM_001135239.1:c.*4C>G NP_001128711.1:n.*4C>G
NM_001165414.1:c.*4C>G NP_001158886.1:n.*4C>G
NM_001165415.1:c.734C>G NP_001158887.1:p.Ser245Cys
NM_001165416.1:c.*153C>G NP_001158888.1:n.*153C>G
NM_005566.3:c.*4C>G NP_005557.1:n.*4C>G
NR_028500.1:n.1157C>G
NM_005566.4:c.*4C>G MANE Select NP_005557.1:n.*4C>G
NM_001165415.2:c.734C>G NP_001158887.1:p.Ser245Cys
NM_001135239.2:c.*4C>G NP_001128711.1:n.*4C>G
NM_001165414.2:c.*4C>G NP_001158886.1:n.*4C>G
NM_001165416.2:c.*153C>G NP_001158888.1:n.*153C>G
NR_028500.2:n.983C>G