Canonical Allele Identifier: CA1955586590
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407170A= , CM000673.2:g.18407170A= GRCh38
NC_000011.9:g.18428717A= , CM000673.1:g.18428717A= GRCh37
NC_000011.8:g.18385293A= NCBI36
NG_008185.1:g.17736A=

Transcript Alleles

HGVS Amino-acid change
ENST00000422447.8:c.888A= MANE Select ENSP00000395337.3:p.Gly296=
ENST00000227157.8:c.*38A= ENSP00000227157.4:n.*38A=
ENST00000375710.7:n.1755A=
ENST00000379412.9:c.888A= ENSP00000368722.5:p.Gly296=
ENST00000396222.6:c.688-69A= ENSP00000379524.2:n.688-69A=
ENST00000422447.7:c.888A= ENSP00000395337.3:p.Gly296=
ENST00000430553.6:c.714A= ENSP00000406172.2:p.Gly238=
ENST00000538451.1:n.775A=
ENST00000540430.5:c.975A= ENSP00000445175.1:p.Gly325=
ENST00000542179.1:c.888A= ENSP00000445331.1:p.Gly296=
ENST00000545215.5:c.*632A= ENSP00000442637.1:n.*632A=
NM_001135239.1:c.714A= NP_001128711.1:p.Gly238=
NM_001165414.1:c.975A= NP_001158886.1:p.Gly325=
NM_001165415.1:c.688-69A= NP_001158887.1:n.688-69A=
NM_001165416.1:c.*38A= NP_001158888.1:n.*38A=
NM_005566.3:c.888A= NP_005557.1:p.Gly296=
NR_028500.1:n.1042A=
NM_005566.4:c.888A= MANE Select NP_005557.1:p.Gly296=
NM_001165415.2:c.688-69A= NP_001158887.1:n.688-69A=
NM_001135239.2:c.714A= NP_001128711.1:p.Gly238=
NM_001165414.2:c.975A= NP_001158886.1:p.Gly325=
NM_001165416.2:c.*38A= NP_001158888.1:n.*38A=
NR_028500.2:n.868A=