Canonical Allele Identifier: CA379503236
Community Standard Title: NM_005566.4(LDHA):c.315C>T (p.Ser105=)
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18400907C>T , CM000673.2:g.18400907C>T GRCh38
NC_000011.9:g.18422454C>T , CM000673.1:g.18422454C>T GRCh37
NC_000011.8:g.18379030C>T NCBI36
NG_008185.1:g.11473C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005566.4:c.315C>T MANE Select NP_005557.1:p.Ser105=
ENST00000422447.8:c.315C>T MANE Select ENSP00000395337.3:p.Ser105=
NM_001135239.1:c.244+1359C>T NP_001128711.1:n.244+1359C>T
NM_001135239.2:c.244+1359C>T NP_001128711.1:n.244+1359C>T
NM_001165414.1:c.402C>T NP_001158886.1:p.Ser134=
NM_001165414.2:c.402C>T NP_001158886.1:p.Ser134=
NM_001165415.1:c.315C>T NP_001158887.1:p.Ser105=
NM_001165415.2:c.315C>T NP_001158887.1:p.Ser105=
NM_001165416.1:c.315C>T NP_001158888.1:p.Ser105=
NM_001165416.2:c.315C>T NP_001158888.1:p.Ser105=
NM_005566.3:c.315C>T NP_005557.1:p.Ser105=
NR_028500.1:n.469C>T
NR_028500.2:n.295C>T
ENST00000227157.8:c.315C>T ENSP00000227157.4:p.Ser105=
ENST00000375710.7:n.1182C>T
ENST00000379412.9:c.315C>T ENSP00000368722.5:p.Ser105=
ENST00000396222.6:c.315C>T ENSP00000379524.2:p.Ser105=
ENST00000422447.7:c.315C>T ENSP00000395337.3:p.Ser105=
ENST00000430553.6:c.244+1359C>T ENSP00000406172.2:n.244+1359C>T
ENST00000460405.5:n.312C>T
ENST00000478970.6:c.315C>T ENSP00000441241.1:p.Ser105=
ENST00000486690.6:c.*59C>T ENSP00000441699.1:n.*59C>T
ENST00000495052.5:c.315C>T ENSP00000446415.1:p.Ser105=
ENST00000536528.5:c.127-1933C>T ENSP00000441058.1:n.127-1933C>T
ENST00000537296.5:n.990C>T
ENST00000539814.5:c.*146C>T ENSP00000442979.1:n.*146C>T
ENST00000540430.5:c.402C>T ENSP00000445175.1:p.Ser134=
ENST00000541097.5:c.244+1359C>T ENSP00000443362.1:n.244+1359C>T
ENST00000542179.1:c.315C>T ENSP00000445331.1:p.Ser105=
ENST00000543445.5:c.315C>T ENSP00000440161.1:p.Ser105=
ENST00000543695.5:c.113C>T ENSP00000440368.1:p.Thr38Ile
ENST00000545215.5:c.*59C>T ENSP00000442637.1:n.*59C>T
ENST00000625635.1:c.113C>T ENSP00000486249.1:p.Thr38Ile