Canonical Allele Identifier: CA674319449

Gene: LDHA

Linked Data

• dbSNP Id: rs1321971504
• gnomAD v4: 11-18407420-G-A
• MyVariant Identifiers: chr11:g.18428967G>A (hg19) ; chr11:g.18407420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407420G>A , CM000673.2:g.18407420G>A	GRCh38
NC_000011.9:g.18428967G>A , CM000673.1:g.18428967G>A	GRCh37
NC_000011.8:g.18385543G>A	NCBI36
NG_008185.1:g.17986G>A
NG_011816.1:g.115G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*139G>A MANE Select	ENSP00000395337.3:n.*139G>A
ENST00000227157.8:c.*288G>A	ENSP00000227157.4:n.*288G>A
ENST00000375710.7:n.2005G>A
ENST00000379412.9:c.*139G>A	ENSP00000368722.5:n.*139G>A
ENST00000396222.6:c.*44G>A	ENSP00000379524.2:n.*44G>A
ENST00000422447.7:c.*139G>A	ENSP00000395337.3:n.*139G>A
ENST00000430553.6:c.*139G>A	ENSP00000406172.2:n.*139G>A
ENST00000538451.1:n.1025G>A
ENST00000540430.5:c.*139G>A	ENSP00000445175.1:n.*139G>A
ENST00000545215.5:c.*882G>A	ENSP00000442637.1:n.*882G>A
NM_001135239.1:c.*139G>A	NP_001128711.1:n.*139G>A
NM_001165414.1:c.*139G>A	NP_001158886.1:n.*139G>A
NM_001165415.1:c.*44G>A	NP_001158887.1:n.*44G>A
NM_001165416.1:c.*288G>A	NP_001158888.1:n.*288G>A
NM_005566.3:c.*139G>A	NP_005557.1:n.*139G>A
NR_028500.1:n.1292G>A
NM_005566.4:c.*139G>A MANE Select	NP_005557.1:n.*139G>A
NM_001165415.2:c.*44G>A	NP_001158887.1:n.*44G>A
NM_001135239.2:c.*139G>A	NP_001128711.1:n.*139G>A
NM_001165414.2:c.*139G>A	NP_001158886.1:n.*139G>A
NM_001165416.2:c.*288G>A	NP_001158888.1:n.*288G>A
NR_028500.2:n.1118G>A