Canonical Allele Identifier: CA2790618550
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407325del , CM000673.2:g.18407325del GRCh38
NC_000011.9:g.18428872del , CM000673.1:g.18428872del GRCh37
NC_000011.8:g.18385448del NCBI36
NG_008185.1:g.17891del
NG_011816.1:g.20del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*44del MANE Select ENSP00000395337.3:n.*44del
ENST00000227157.8:c.*193del ENSP00000227157.4:n.*193del
ENST00000375710.7:n.1910del
ENST00000379412.9:c.*44del ENSP00000368722.5:n.*44del
ENST00000396222.6:c.774del ENSP00000379524.2:p.Ile259PhefsTer2
ENST00000422447.7:c.*44del ENSP00000395337.3:n.*44del
ENST00000430553.6:c.*44del ENSP00000406172.2:n.*44del
ENST00000538451.1:n.930del
ENST00000540430.5:c.*44del ENSP00000445175.1:n.*44del
ENST00000545215.5:c.*787del ENSP00000442637.1:n.*787del
NM_001135239.1:c.*44del NP_001128711.1:n.*44del
NM_001165414.1:c.*44del NP_001158886.1:n.*44del
NM_001165415.1:c.774del NP_001158887.1:p.Ile259PhefsTer2
NM_001165416.1:c.*193del NP_001158888.1:n.*193del
NM_005566.3:c.*44del NP_005557.1:n.*44del
NR_028500.1:n.1197del
NM_005566.4:c.*44del MANE Select NP_005557.1:n.*44del
NM_001165415.2:c.774del NP_001158887.1:p.Ile259PhefsTer2
NM_001135239.2:c.*44del NP_001128711.1:n.*44del
NM_001165414.2:c.*44del NP_001158886.1:n.*44del
NM_001165416.2:c.*193del NP_001158888.1:n.*193del
NR_028500.2:n.1023del