Canonical Allele Identifier: CA1955586587

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407161C= , CM000673.2:g.18407161C=	GRCh38
NC_000011.9:g.18428708C= , CM000673.1:g.18428708C=	GRCh37
NC_000011.8:g.18385284C=	NCBI36
NG_008185.1:g.17727C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.879C= MANE Select	ENSP00000395337.3:p.Cys293=
ENST00000227157.8:c.*29C=	ENSP00000227157.4:n.*29C=
ENST00000375710.7:n.1746C=
ENST00000379412.9:c.879C=	ENSP00000368722.5:p.Cys293=
ENST00000396222.6:c.688-78C=	ENSP00000379524.2:n.688-78C=
ENST00000422447.7:c.879C=	ENSP00000395337.3:p.Cys293=
ENST00000430553.6:c.705C=	ENSP00000406172.2:p.Cys235=
ENST00000538451.1:n.766C=
ENST00000540430.5:c.966C=	ENSP00000445175.1:p.Cys322=
ENST00000542179.1:c.879C=	ENSP00000445331.1:p.Cys293=
ENST00000545215.5:c.*623C=	ENSP00000442637.1:n.*623C=
NM_001135239.1:c.705C=	NP_001128711.1:p.Cys235=
NM_001165414.1:c.966C=	NP_001158886.1:p.Cys322=
NM_001165415.1:c.688-78C=	NP_001158887.1:n.688-78C=
NM_001165416.1:c.*29C=	NP_001158888.1:n.*29C=
NM_005566.3:c.879C=	NP_005557.1:p.Cys293=
NR_028500.1:n.1033C=
NM_005566.4:c.879C= MANE Select	NP_005557.1:p.Cys293=
NM_001165415.2:c.688-78C=	NP_001158887.1:n.688-78C=
NM_001135239.2:c.705C=	NP_001128711.1:p.Cys235=
NM_001165414.2:c.966C=	NP_001158886.1:p.Cys322=
NM_001165416.2:c.*29C=	NP_001158888.1:n.*29C=
NR_028500.2:n.859C=