Canonical Allele Identifier: CA379509552
Gene: LDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407288C>T , CM000673.2:g.18407288C>T GRCh38
NC_000011.9:g.18428835C>T , CM000673.1:g.18428835C>T GRCh37
NC_000011.8:g.18385411C>T NCBI36
NG_008185.1:g.17854C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*7C>T MANE Select ENSP00000395337.3:n.*7C>T
ENST00000227157.8:c.*156C>T ENSP00000227157.4:n.*156C>T
ENST00000375710.7:n.1873C>T
ENST00000379412.9:c.*7C>T ENSP00000368722.5:n.*7C>T
ENST00000396222.6:c.737C>T ENSP00000379524.2:p.Ser246Phe
ENST00000422447.7:c.*7C>T ENSP00000395337.3:n.*7C>T
ENST00000430553.6:c.*7C>T ENSP00000406172.2:n.*7C>T
ENST00000538451.1:n.893C>T
ENST00000540430.5:c.*7C>T ENSP00000445175.1:n.*7C>T
ENST00000545215.5:c.*750C>T ENSP00000442637.1:n.*750C>T
NM_001135239.1:c.*7C>T NP_001128711.1:n.*7C>T
NM_001165414.1:c.*7C>T NP_001158886.1:n.*7C>T
NM_001165415.1:c.737C>T NP_001158887.1:p.Ser246Phe
NM_001165416.1:c.*156C>T NP_001158888.1:n.*156C>T
NM_005566.3:c.*7C>T NP_005557.1:n.*7C>T
NR_028500.1:n.1160C>T
NM_005566.4:c.*7C>T MANE Select NP_005557.1:n.*7C>T
NM_001165415.2:c.737C>T NP_001158887.1:p.Ser246Phe
NM_001135239.2:c.*7C>T NP_001128711.1:n.*7C>T
NM_001165414.2:c.*7C>T NP_001158886.1:n.*7C>T
NM_001165416.2:c.*156C>T NP_001158888.1:n.*156C>T
NR_028500.2:n.986C>T