Canonical Allele Identifier: CA379510197

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428897T>A (hg19) ; chr11:g.18407350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407350T>A , CM000673.2:g.18407350T>A	GRCh38
NC_000011.9:g.18428897T>A , CM000673.1:g.18428897T>A	GRCh37
NC_000011.8:g.18385473T>A	NCBI36
NG_008185.1:g.17916T>A
NG_011816.1:g.45T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*69T>A MANE Select	ENSP00000395337.3:n.*69T>A
ENST00000227157.8:c.*218T>A	ENSP00000227157.4:n.*218T>A
ENST00000375710.7:n.1935T>A
ENST00000379412.9:c.*69T>A	ENSP00000368722.5:n.*69T>A
ENST00000396222.6:c.799T>A	ENSP00000379524.2:p.Cys267Ser
ENST00000422447.7:c.*69T>A	ENSP00000395337.3:n.*69T>A
ENST00000430553.6:c.*69T>A	ENSP00000406172.2:n.*69T>A
ENST00000538451.1:n.955T>A
ENST00000540430.5:c.*69T>A	ENSP00000445175.1:n.*69T>A
ENST00000545215.5:c.*812T>A	ENSP00000442637.1:n.*812T>A
NM_001135239.1:c.*69T>A	NP_001128711.1:n.*69T>A
NM_001165414.1:c.*69T>A	NP_001158886.1:n.*69T>A
NM_001165415.1:c.799T>A	NP_001158887.1:p.Cys267Ser
NM_001165416.1:c.*218T>A	NP_001158888.1:n.*218T>A
NM_005566.3:c.*69T>A	NP_005557.1:n.*69T>A
NR_028500.1:n.1222T>A
NM_005566.4:c.*69T>A MANE Select	NP_005557.1:n.*69T>A
NM_001165415.2:c.799T>A	NP_001158887.1:p.Cys267Ser
NM_001135239.2:c.*69T>A	NP_001128711.1:n.*69T>A
NM_001165414.2:c.*69T>A	NP_001158886.1:n.*69T>A
NM_001165416.2:c.*218T>A	NP_001158888.1:n.*218T>A
NR_028500.2:n.1048T>A