Canonical Allele Identifier: CA1955586658

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407332G= , CM000673.2:g.18407332G=	GRCh38
NC_000011.9:g.18428879G= , CM000673.1:g.18428879G=	GRCh37
NC_000011.8:g.18385455G=	NCBI36
NG_008185.1:g.17898G=
NG_011816.1:g.27G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*51G= MANE Select	ENSP00000395337.3:n.*51G=
ENST00000227157.8:c.*200G=	ENSP00000227157.4:n.*200G=
ENST00000375710.7:n.1917G=
ENST00000379412.9:c.*51G=	ENSP00000368722.5:n.*51G=
ENST00000396222.6:c.781G=	ENSP00000379524.2:p.Gly261=
ENST00000422447.7:c.*51G=	ENSP00000395337.3:n.*51G=
ENST00000430553.6:c.*51G=	ENSP00000406172.2:n.*51G=
ENST00000538451.1:n.937G=
ENST00000540430.5:c.*51G=	ENSP00000445175.1:n.*51G=
ENST00000545215.5:c.*794G=	ENSP00000442637.1:n.*794G=
NM_001135239.1:c.*51G=	NP_001128711.1:n.*51G=
NM_001165414.1:c.*51G=	NP_001158886.1:n.*51G=
NM_001165415.1:c.781G=	NP_001158887.1:p.Gly261=
NM_001165416.1:c.*200G=	NP_001158888.1:n.*200G=
NM_005566.3:c.*51G=	NP_005557.1:n.*51G=
NR_028500.1:n.1204G=
NM_005566.4:c.*51G= MANE Select	NP_005557.1:n.*51G=
NM_001165415.2:c.781G=	NP_001158887.1:p.Gly261=
NM_001135239.2:c.*51G=	NP_001128711.1:n.*51G=
NM_001165414.2:c.*51G=	NP_001158886.1:n.*51G=
NM_001165416.2:c.*200G=	NP_001158888.1:n.*200G=
NR_028500.2:n.1030G=