Canonical Allele Identifier: CA1955586708
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407444T= , CM000673.2:g.18407444T= GRCh38
NC_000011.9:g.18428991T= , CM000673.1:g.18428991T= GRCh37
NC_000011.8:g.18385567T= NCBI36
NG_008185.1:g.18010T=
NG_011816.1:g.139T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*163T= MANE Select ENSP00000395337.3:n.*163T=
ENST00000227157.8:c.*312T= ENSP00000227157.4:n.*312T=
ENST00000375710.7:n.2029T=
ENST00000379412.9:c.*163T= ENSP00000368722.5:n.*163T=
ENST00000396222.6:c.*68T= ENSP00000379524.2:n.*68T=
ENST00000422447.7:c.*163T= ENSP00000395337.3:n.*163T=
ENST00000430553.6:c.*163T= ENSP00000406172.2:n.*163T=
ENST00000538451.1:n.1049T=
ENST00000540430.5:c.*163T= ENSP00000445175.1:n.*163T=
ENST00000545215.5:c.*906T= ENSP00000442637.1:n.*906T=
NM_001135239.1:c.*163T= NP_001128711.1:n.*163T=
NM_001165414.1:c.*163T= NP_001158886.1:n.*163T=
NM_001165415.1:c.*68T= NP_001158887.1:n.*68T=
NM_001165416.1:c.*312T= NP_001158888.1:n.*312T=
NM_005566.3:c.*163T= NP_005557.1:n.*163T=
NR_028500.1:n.1316T=
NM_005566.4:c.*163T= MANE Select NP_005557.1:n.*163T=
NM_001165415.2:c.*68T= NP_001158887.1:n.*68T=
NM_001135239.2:c.*163T= NP_001128711.1:n.*163T=
NM_001165414.2:c.*163T= NP_001158886.1:n.*163T=
NM_001165416.2:c.*312T= NP_001158888.1:n.*312T=
NR_028500.2:n.1142T=