Canonical Allele Identifier: CA379508782

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428713T>G (hg19) ; chr11:g.18407166T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407166T>G , CM000673.2:g.18407166T>G	GRCh38
NC_000011.9:g.18428713T>G , CM000673.1:g.18428713T>G	GRCh37
NC_000011.8:g.18385289T>G	NCBI36
NG_008185.1:g.17732T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.884T>G MANE Select	ENSP00000395337.3:p.Leu295Trp
ENST00000227157.8:c.*34T>G	ENSP00000227157.4:n.*34T>G
ENST00000375710.7:n.1751T>G
ENST00000379412.9:c.884T>G	ENSP00000368722.5:p.Leu295Trp
ENST00000396222.6:c.688-73T>G	ENSP00000379524.2:n.688-73T>G
ENST00000422447.7:c.884T>G	ENSP00000395337.3:p.Leu295Trp
ENST00000430553.6:c.710T>G	ENSP00000406172.2:p.Leu237Trp
ENST00000538451.1:n.771T>G
ENST00000540430.5:c.971T>G	ENSP00000445175.1:p.Leu324Trp
ENST00000542179.1:c.884T>G	ENSP00000445331.1:p.Leu295Trp
ENST00000545215.5:c.*628T>G	ENSP00000442637.1:n.*628T>G
NM_001135239.1:c.710T>G	NP_001128711.1:p.Leu237Trp
NM_001165414.1:c.971T>G	NP_001158886.1:p.Leu324Trp
NM_001165415.1:c.688-73T>G	NP_001158887.1:n.688-73T>G
NM_001165416.1:c.*34T>G	NP_001158888.1:n.*34T>G
NM_005566.3:c.884T>G	NP_005557.1:p.Leu295Trp
NR_028500.1:n.1038T>G
NM_005566.4:c.884T>G MANE Select	NP_005557.1:p.Leu295Trp
NM_001165415.2:c.688-73T>G	NP_001158887.1:n.688-73T>G
NM_001135239.2:c.710T>G	NP_001128711.1:p.Leu237Trp
NM_001165414.2:c.971T>G	NP_001158886.1:p.Leu324Trp
NM_001165416.2:c.*34T>G	NP_001158888.1:n.*34T>G
NR_028500.2:n.864T>G