Canonical Allele Identifier: CA379503369
Community Standard Title: NM_005566.4(LDHA):c.340G>A (p.Val114Met)
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18400932G>A , CM000673.2:g.18400932G>A GRCh38
NC_000011.9:g.18422479G>A , CM000673.1:g.18422479G>A GRCh37
NC_000011.8:g.18379055G>A NCBI36
NG_008185.1:g.11498G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005566.4:c.340G>A MANE Select NP_005557.1:p.Val114Met
ENST00000422447.8:c.340G>A MANE Select ENSP00000395337.3:p.Val114Met
NM_001135239.1:c.244+1384G>A NP_001128711.1:n.244+1384G>A
NM_001135239.2:c.244+1384G>A NP_001128711.1:n.244+1384G>A
NM_001165414.1:c.427G>A NP_001158886.1:p.Val143Met
NM_001165414.2:c.427G>A NP_001158886.1:p.Val143Met
NM_001165415.1:c.340G>A NP_001158887.1:p.Val114Met
NM_001165415.2:c.340G>A NP_001158887.1:p.Val114Met
NM_001165416.1:c.340G>A NP_001158888.1:p.Val114Met
NM_001165416.2:c.340G>A NP_001158888.1:p.Val114Met
NM_005566.3:c.340G>A NP_005557.1:p.Val114Met
NR_028500.1:n.494G>A
NR_028500.2:n.320G>A
ENST00000227157.8:c.340G>A ENSP00000227157.4:p.Val114Met
ENST00000375710.7:n.1207G>A
ENST00000379412.9:c.340G>A ENSP00000368722.5:p.Val114Met
ENST00000396222.6:c.340G>A ENSP00000379524.2:p.Val114Met
ENST00000422447.7:c.340G>A ENSP00000395337.3:p.Val114Met
ENST00000430553.6:c.244+1384G>A ENSP00000406172.2:n.244+1384G>A
ENST00000460405.5:n.337G>A
ENST00000478970.6:c.340G>A ENSP00000441241.1:p.Val114Met
ENST00000486690.6:c.*84G>A ENSP00000441699.1:n.*84G>A
ENST00000495052.5:c.340G>A ENSP00000446415.1:p.Val114Met
ENST00000536528.5:c.127-1908G>A ENSP00000441058.1:n.127-1908G>A
ENST00000537296.5:n.1015G>A
ENST00000539814.5:c.*171G>A ENSP00000442979.1:n.*171G>A
ENST00000540430.5:c.427G>A ENSP00000445175.1:p.Val143Met
ENST00000541097.5:c.244+1384G>A ENSP00000443362.1:n.244+1384G>A
ENST00000542179.1:c.340G>A ENSP00000445331.1:p.Val114Met
ENST00000543445.5:c.340G>A ENSP00000440161.1:p.Val114Met
ENST00000543695.5:c.138G>A ENSP00000440368.1:p.Thr46=
ENST00000545215.5:c.*84G>A ENSP00000442637.1:n.*84G>A
ENST00000625635.1:c.138G>A ENSP00000486249.1:p.Thr46=