Canonical Allele Identifier: CA379509365

Gene: LDHA

Linked Data

• dbSNP Id: rs1866723015
• MyVariant Identifiers: chr11:g.18428816G>A (hg19) ; chr11:g.18407269G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407269G>A , CM000673.2:g.18407269G>A	GRCh38
NC_000011.9:g.18428816G>A , CM000673.1:g.18428816G>A	GRCh37
NC_000011.8:g.18385392G>A	NCBI36
NG_008185.1:g.17835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.987G>A MANE Select	ENSP00000395337.3:p.Glu329=
ENST00000227157.8:c.*137G>A	ENSP00000227157.4:n.*137G>A
ENST00000375710.7:n.1854G>A
ENST00000379412.9:c.987G>A	ENSP00000368722.5:p.Glu329=
ENST00000396222.6:c.718G>A	ENSP00000379524.2:p.Ala240Thr
ENST00000422447.7:c.987G>A	ENSP00000395337.3:p.Glu329=
ENST00000430553.6:c.813G>A	ENSP00000406172.2:p.Glu271=
ENST00000538451.1:n.874G>A
ENST00000540430.5:c.1074G>A	ENSP00000445175.1:p.Glu358=
ENST00000542179.1:c.987G>A	ENSP00000445331.1:p.Glu329=
ENST00000545215.5:c.*731G>A	ENSP00000442637.1:n.*731G>A
NM_001135239.1:c.813G>A	NP_001128711.1:p.Glu271=
NM_001165414.1:c.1074G>A	NP_001158886.1:p.Glu358=
NM_001165415.1:c.718G>A	NP_001158887.1:p.Ala240Thr
NM_001165416.1:c.*137G>A	NP_001158888.1:n.*137G>A
NM_005566.3:c.987G>A	NP_005557.1:p.Glu329=
NR_028500.1:n.1141G>A
NM_005566.4:c.987G>A MANE Select	NP_005557.1:p.Glu329=
NM_001165415.2:c.718G>A	NP_001158887.1:p.Ala240Thr
NM_001135239.2:c.813G>A	NP_001128711.1:p.Glu271=
NM_001165414.2:c.1074G>A	NP_001158886.1:p.Glu358=
NM_001165416.2:c.*137G>A	NP_001158888.1:n.*137G>A
NR_028500.2:n.967G>A