Canonical Allele Identifier: CA1955586690
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407395T= , CM000673.2:g.18407395T= GRCh38
NC_000011.9:g.18428942T= , CM000673.1:g.18428942T= GRCh37
NC_000011.8:g.18385518T= NCBI36
NG_008185.1:g.17961T=
NG_011816.1:g.90T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*114T= MANE Select ENSP00000395337.3:n.*114T=
ENST00000227157.8:c.*263T= ENSP00000227157.4:n.*263T=
ENST00000375710.7:n.1980T=
ENST00000379412.9:c.*114T= ENSP00000368722.5:n.*114T=
ENST00000396222.6:c.*19T= ENSP00000379524.2:n.*19T=
ENST00000422447.7:c.*114T= ENSP00000395337.3:n.*114T=
ENST00000430553.6:c.*114T= ENSP00000406172.2:n.*114T=
ENST00000538451.1:n.1000T=
ENST00000540430.5:c.*114T= ENSP00000445175.1:n.*114T=
ENST00000545215.5:c.*857T= ENSP00000442637.1:n.*857T=
NM_001135239.1:c.*114T= NP_001128711.1:n.*114T=
NM_001165414.1:c.*114T= NP_001158886.1:n.*114T=
NM_001165415.1:c.*19T= NP_001158887.1:n.*19T=
NM_001165416.1:c.*263T= NP_001158888.1:n.*263T=
NM_005566.3:c.*114T= NP_005557.1:n.*114T=
NR_028500.1:n.1267T=
NM_005566.4:c.*114T= MANE Select NP_005557.1:n.*114T=
NM_001165415.2:c.*19T= NP_001158887.1:n.*19T=
NM_001135239.2:c.*114T= NP_001128711.1:n.*114T=
NM_001165414.2:c.*114T= NP_001158886.1:n.*114T=
NM_001165416.2:c.*263T= NP_001158888.1:n.*263T=
NR_028500.2:n.1093T=