Canonical Allele Identifier: CA1955586589
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407169G= , CM000673.2:g.18407169G= GRCh38
NC_000011.9:g.18428716G= , CM000673.1:g.18428716G= GRCh37
NC_000011.8:g.18385292G= NCBI36
NG_008185.1:g.17735G=

Transcript Alleles

HGVS Amino-acid change
ENST00000422447.8:c.887G= MANE Select ENSP00000395337.3:p.Gly296=
ENST00000227157.8:c.*37G= ENSP00000227157.4:n.*37G=
ENST00000375710.7:n.1754G=
ENST00000379412.9:c.887G= ENSP00000368722.5:p.Gly296=
ENST00000396222.6:c.688-70G= ENSP00000379524.2:n.688-70G=
ENST00000422447.7:c.887G= ENSP00000395337.3:p.Gly296=
ENST00000430553.6:c.713G= ENSP00000406172.2:p.Gly238=
ENST00000538451.1:n.774G=
ENST00000540430.5:c.974G= ENSP00000445175.1:p.Gly325=
ENST00000542179.1:c.887G= ENSP00000445331.1:p.Gly296=
ENST00000545215.5:c.*631G= ENSP00000442637.1:n.*631G=
NM_001135239.1:c.713G= NP_001128711.1:p.Gly238=
NM_001165414.1:c.974G= NP_001158886.1:p.Gly325=
NM_001165415.1:c.688-70G= NP_001158887.1:n.688-70G=
NM_001165416.1:c.*37G= NP_001158888.1:n.*37G=
NM_005566.3:c.887G= NP_005557.1:p.Gly296=
NR_028500.1:n.1041G=
NM_005566.4:c.887G= MANE Select NP_005557.1:p.Gly296=
NM_001165415.2:c.688-70G= NP_001158887.1:n.688-70G=
NM_001135239.2:c.713G= NP_001128711.1:p.Gly238=
NM_001165414.2:c.974G= NP_001158886.1:p.Gly325=
NM_001165416.2:c.*37G= NP_001158888.1:n.*37G=
NR_028500.2:n.867G=