Canonical Allele Identifier: CA1955586666
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407344G= , CM000673.2:g.18407344G= GRCh38
NC_000011.9:g.18428891G= , CM000673.1:g.18428891G= GRCh37
NC_000011.8:g.18385467G= NCBI36
NG_008185.1:g.17910G=
NG_011816.1:g.39G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*63G= MANE Select ENSP00000395337.3:n.*63G=
ENST00000227157.8:c.*212G= ENSP00000227157.4:n.*212G=
ENST00000375710.7:n.1929G=
ENST00000379412.9:c.*63G= ENSP00000368722.5:n.*63G=
ENST00000396222.6:c.793G= ENSP00000379524.2:p.Ala265=
ENST00000422447.7:c.*63G= ENSP00000395337.3:n.*63G=
ENST00000430553.6:c.*63G= ENSP00000406172.2:n.*63G=
ENST00000538451.1:n.949G=
ENST00000540430.5:c.*63G= ENSP00000445175.1:n.*63G=
ENST00000545215.5:c.*806G= ENSP00000442637.1:n.*806G=
NM_001135239.1:c.*63G= NP_001128711.1:n.*63G=
NM_001165414.1:c.*63G= NP_001158886.1:n.*63G=
NM_001165415.1:c.793G= NP_001158887.1:p.Ala265=
NM_001165416.1:c.*212G= NP_001158888.1:n.*212G=
NM_005566.3:c.*63G= NP_005557.1:n.*63G=
NR_028500.1:n.1216G=
NM_005566.4:c.*63G= MANE Select NP_005557.1:n.*63G=
NM_001165415.2:c.793G= NP_001158887.1:p.Ala265=
NM_001135239.2:c.*63G= NP_001128711.1:n.*63G=
NM_001165414.2:c.*63G= NP_001158886.1:n.*63G=
NM_001165416.2:c.*212G= NP_001158888.1:n.*212G=
NR_028500.2:n.1042G=