Canonical Allele Identifier: CA5911435

Gene: LDHA

Linked Data

• dbSNP Id: rs776605053
• ExAC: 11:18428717 A / G
• gnomAD v2: 11-18428717-A-G
• MyVariant Identifiers: chr11:g.18428717A>G (hg19) ; chr11:g.18407170A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407170A>G , CM000673.2:g.18407170A>G	GRCh38
NC_000011.9:g.18428717A>G , CM000673.1:g.18428717A>G	GRCh37
NC_000011.8:g.18385293A>G	NCBI36
NG_008185.1:g.17736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.888A>G MANE Select	ENSP00000395337.3:p.Gly296=
ENST00000227157.8:c.*38A>G	ENSP00000227157.4:n.*38A>G
ENST00000375710.7:n.1755A>G
ENST00000379412.9:c.888A>G	ENSP00000368722.5:p.Gly296=
ENST00000396222.6:c.688-69A>G	ENSP00000379524.2:n.688-69A>G
ENST00000422447.7:c.888A>G	ENSP00000395337.3:p.Gly296=
ENST00000430553.6:c.714A>G	ENSP00000406172.2:p.Gly238=
ENST00000538451.1:n.775A>G
ENST00000540430.5:c.975A>G	ENSP00000445175.1:p.Gly325=
ENST00000542179.1:c.888A>G	ENSP00000445331.1:p.Gly296=
ENST00000545215.5:c.*632A>G	ENSP00000442637.1:n.*632A>G
NM_001135239.1:c.714A>G	NP_001128711.1:p.Gly238=
NM_001165414.1:c.975A>G	NP_001158886.1:p.Gly325=
NM_001165415.1:c.688-69A>G	NP_001158887.1:n.688-69A>G
NM_001165416.1:c.*38A>G	NP_001158888.1:n.*38A>G
NM_005566.3:c.888A>G	NP_005557.1:p.Gly296=
NR_028500.1:n.1042A>G
NM_005566.4:c.888A>G MANE Select	NP_005557.1:p.Gly296=
NM_001165415.2:c.688-69A>G	NP_001158887.1:n.688-69A>G
NM_001135239.2:c.714A>G	NP_001128711.1:p.Gly238=
NM_001165414.2:c.975A>G	NP_001158886.1:p.Gly325=
NM_001165416.2:c.*38A>G	NP_001158888.1:n.*38A>G
NR_028500.2:n.868A>G