Canonical Allele Identifier: CA2612742068

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407456-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407456C>A , CM000673.2:g.18407456C>A	GRCh38
NC_000011.9:g.18429003C>A , CM000673.1:g.18429003C>A	GRCh37
NC_000011.8:g.18385579C>A	NCBI36
NG_008185.1:g.18022C>A
NG_011816.1:g.151C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*175C>A MANE Select	ENSP00000395337.3:n.*175C>A
ENST00000227157.8:c.*324C>A	ENSP00000227157.4:n.*324C>A
ENST00000375710.7:n.2041C>A
ENST00000379412.9:c.*175C>A	ENSP00000368722.5:n.*175C>A
ENST00000396222.6:c.*80C>A	ENSP00000379524.2:n.*80C>A
ENST00000422447.7:c.*175C>A	ENSP00000395337.3:n.*175C>A
ENST00000430553.6:c.*175C>A	ENSP00000406172.2:n.*175C>A
ENST00000538451.1:n.1061C>A
ENST00000540430.5:c.*175C>A	ENSP00000445175.1:n.*175C>A
ENST00000545215.5:c.*918C>A	ENSP00000442637.1:n.*918C>A
NM_001135239.1:c.*175C>A	NP_001128711.1:n.*175C>A
NM_001165414.1:c.*175C>A	NP_001158886.1:n.*175C>A
NM_001165415.1:c.*80C>A	NP_001158887.1:n.*80C>A
NM_001165416.1:c.*324C>A	NP_001158888.1:n.*324C>A
NM_005566.3:c.*175C>A	NP_005557.1:n.*175C>A
NR_028500.1:n.1328C>A
NM_005566.4:c.*175C>A MANE Select	NP_005557.1:n.*175C>A
NM_001165415.2:c.*80C>A	NP_001158887.1:n.*80C>A
NM_001135239.2:c.*175C>A	NP_001128711.1:n.*175C>A
NM_001165414.2:c.*175C>A	NP_001158886.1:n.*175C>A
NM_001165416.2:c.*324C>A	NP_001158888.1:n.*324C>A
NR_028500.2:n.1154C>A