Canonical Allele Identifier: CA379510097

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407343-T-G
• MyVariant Identifiers: chr11:g.18428890T>G (hg19) ; chr11:g.18407343T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407343T>G , CM000673.2:g.18407343T>G	GRCh38
NC_000011.9:g.18428890T>G , CM000673.1:g.18428890T>G	GRCh37
NC_000011.8:g.18385466T>G	NCBI36
NG_008185.1:g.17909T>G
NG_011816.1:g.38T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*62T>G MANE Select	ENSP00000395337.3:n.*62T>G
ENST00000227157.8:c.*211T>G	ENSP00000227157.4:n.*211T>G
ENST00000375710.7:n.1928T>G
ENST00000379412.9:c.*62T>G	ENSP00000368722.5:n.*62T>G
ENST00000396222.6:c.792T>G	ENSP00000379524.2:p.Cys264Trp
ENST00000422447.7:c.*62T>G	ENSP00000395337.3:n.*62T>G
ENST00000430553.6:c.*62T>G	ENSP00000406172.2:n.*62T>G
ENST00000538451.1:n.948T>G
ENST00000540430.5:c.*62T>G	ENSP00000445175.1:n.*62T>G
ENST00000545215.5:c.*805T>G	ENSP00000442637.1:n.*805T>G
NM_001135239.1:c.*62T>G	NP_001128711.1:n.*62T>G
NM_001165414.1:c.*62T>G	NP_001158886.1:n.*62T>G
NM_001165415.1:c.792T>G	NP_001158887.1:p.Cys264Trp
NM_001165416.1:c.*211T>G	NP_001158888.1:n.*211T>G
NM_005566.3:c.*62T>G	NP_005557.1:n.*62T>G
NR_028500.1:n.1215T>G
NM_005566.4:c.*62T>G MANE Select	NP_005557.1:n.*62T>G
NM_001165415.2:c.792T>G	NP_001158887.1:p.Cys264Trp
NM_001135239.2:c.*62T>G	NP_001128711.1:n.*62T>G
NM_001165414.2:c.*62T>G	NP_001158886.1:n.*62T>G
NM_001165416.2:c.*211T>G	NP_001158888.1:n.*211T>G
NR_028500.2:n.1041T>G