Canonical Allele Identifier: CA379509539
Gene: LDHA HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*4C>A MANE Select ENSP00000395337.3:n.*4C>A
ENST00000227157.8:c.*153C>A ENSP00000227157.4:n.*153C>A
ENST00000375710.7:n.1870C>A
ENST00000379412.9:c.*4C>A ENSP00000368722.5:n.*4C>A
ENST00000396222.6:c.734C>A ENSP00000379524.2:p.Ser245Tyr
ENST00000422447.7:c.*4C>A ENSP00000395337.3:n.*4C>A
ENST00000430553.6:c.*4C>A ENSP00000406172.2:n.*4C>A
ENST00000538451.1:n.890C>A
ENST00000540430.5:c.*4C>A ENSP00000445175.1:n.*4C>A
ENST00000545215.5:c.*747C>A ENSP00000442637.1:n.*747C>A
NM_001135239.1:c.*4C>A NP_001128711.1:n.*4C>A
NM_001165414.1:c.*4C>A NP_001158886.1:n.*4C>A
NM_001165415.1:c.734C>A NP_001158887.1:p.Ser245Tyr
NM_001165416.1:c.*153C>A NP_001158888.1:n.*153C>A
NM_005566.3:c.*4C>A NP_005557.1:n.*4C>A
NR_028500.1:n.1157C>A
NM_005566.4:c.*4C>A MANE Select NP_005557.1:n.*4C>A
NM_001165415.2:c.734C>A NP_001158887.1:p.Ser245Tyr
NM_001135239.2:c.*4C>A NP_001128711.1:n.*4C>A
NM_001165414.2:c.*4C>A NP_001158886.1:n.*4C>A
NM_001165416.2:c.*153C>A NP_001158888.1:n.*153C>A
NR_028500.2:n.983C>A