Canonical Allele Identifier: CA218586720

Gene: LDHA

Linked Data

• dbSNP Id: rs928802169
• gnomAD v3: 11-18407473-A-AT
• gnomAD v4: 11-18407473-A-AT
• MyVariant Identifiers: chr11:g.18429020_18429021insT (hg19) ; chr11:g.18407473_18407474insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407474dup , CM000673.2:g.18407474dup	GRCh38
NC_000011.9:g.18429021dup , CM000673.1:g.18429021dup	GRCh37
NC_000011.8:g.18385597dup	NCBI36
NG_008185.1:g.18040dup
NG_011816.1:g.169dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*193dup MANE Select	ENSP00000395337.3:n.*193dup
ENST00000227157.8:c.*342dup	ENSP00000227157.4:n.*342dup
ENST00000375710.7:n.2059dup
ENST00000379412.9:c.*193dup	ENSP00000368722.5:n.*193dup
ENST00000396222.6:c.*98dup	ENSP00000379524.2:n.*98dup
ENST00000422447.7:c.*193dup	ENSP00000395337.3:n.*193dup
ENST00000430553.6:c.*193dup	ENSP00000406172.2:n.*193dup
ENST00000538451.1:n.1079dup
ENST00000540430.5:c.*193dup	ENSP00000445175.1:n.*193dup
ENST00000545215.5:c.*936dup	ENSP00000442637.1:n.*936dup
NM_001135239.1:c.*193dup	NP_001128711.1:n.*193dup
NM_001165414.1:c.*193dup	NP_001158886.1:n.*193dup
NM_001165415.1:c.*98dup	NP_001158887.1:n.*98dup
NM_001165416.1:c.*342dup	NP_001158888.1:n.*342dup
NM_005566.3:c.*193dup	NP_005557.1:n.*193dup
NR_028500.1:n.1346dup
NM_005566.4:c.*193dup MANE Select	NP_005557.1:n.*193dup
NM_001165415.2:c.*98dup	NP_001158887.1:n.*98dup
NM_001135239.2:c.*193dup	NP_001128711.1:n.*193dup
NM_001165414.2:c.*193dup	NP_001158886.1:n.*193dup
NM_001165416.2:c.*342dup	NP_001158888.1:n.*342dup
NR_028500.2:n.1172dup