Canonical Allele Identifier: CA1955586718
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407456C= , CM000673.2:g.18407456C= GRCh38
NC_000011.9:g.18429003C= , CM000673.1:g.18429003C= GRCh37
NC_000011.8:g.18385579C= NCBI36
NG_008185.1:g.18022C=
NG_011816.1:g.151C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*175C= MANE Select ENSP00000395337.3:n.*175C=
ENST00000227157.8:c.*324C= ENSP00000227157.4:n.*324C=
ENST00000375710.7:n.2041C=
ENST00000379412.9:c.*175C= ENSP00000368722.5:n.*175C=
ENST00000396222.6:c.*80C= ENSP00000379524.2:n.*80C=
ENST00000422447.7:c.*175C= ENSP00000395337.3:n.*175C=
ENST00000430553.6:c.*175C= ENSP00000406172.2:n.*175C=
ENST00000538451.1:n.1061C=
ENST00000540430.5:c.*175C= ENSP00000445175.1:n.*175C=
ENST00000545215.5:c.*918C= ENSP00000442637.1:n.*918C=
NM_001135239.1:c.*175C= NP_001128711.1:n.*175C=
NM_001165414.1:c.*175C= NP_001158886.1:n.*175C=
NM_001165415.1:c.*80C= NP_001158887.1:n.*80C=
NM_001165416.1:c.*324C= NP_001158888.1:n.*324C=
NM_005566.3:c.*175C= NP_005557.1:n.*175C=
NR_028500.1:n.1328C=
NM_005566.4:c.*175C= MANE Select NP_005557.1:n.*175C=
NM_001165415.2:c.*80C= NP_001158887.1:n.*80C=
NM_001135239.2:c.*175C= NP_001128711.1:n.*175C=
NM_001165414.2:c.*175C= NP_001158886.1:n.*175C=
NM_001165416.2:c.*324C= NP_001158888.1:n.*324C=
NR_028500.2:n.1154C=