Canonical Allele Identifier: CA379508708

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428691T>G (hg19) ; chr11:g.18407144T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407144T>G , CM000673.2:g.18407144T>G	GRCh38
NC_000011.9:g.18428691T>G , CM000673.1:g.18428691T>G	GRCh37
NC_000011.8:g.18385267T>G	NCBI36
NG_008185.1:g.17710T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.862T>G MANE Select	ENSP00000395337.3:p.Phe288Val
ENST00000227157.8:c.*12T>G	ENSP00000227157.4:n.*12T>G
ENST00000375710.7:n.1729T>G
ENST00000379412.9:c.862T>G	ENSP00000368722.5:p.Phe288Val
ENST00000396222.6:c.688-95T>G	ENSP00000379524.2:n.688-95T>G
ENST00000422447.7:c.862T>G	ENSP00000395337.3:p.Phe288Val
ENST00000430553.6:c.688T>G	ENSP00000406172.2:p.Phe230Val
ENST00000538451.1:n.749T>G
ENST00000540430.5:c.949T>G	ENSP00000445175.1:p.Phe317Val
ENST00000541097.5:c.*200T>G	ENSP00000443362.1:n.*200T>G
ENST00000542179.1:c.862T>G	ENSP00000445331.1:p.Phe288Val
ENST00000545215.5:c.*606T>G	ENSP00000442637.1:n.*606T>G
NM_001135239.1:c.688T>G	NP_001128711.1:p.Phe230Val
NM_001165414.1:c.949T>G	NP_001158886.1:p.Phe317Val
NM_001165415.1:c.688-95T>G	NP_001158887.1:n.688-95T>G
NM_001165416.1:c.*12T>G	NP_001158888.1:n.*12T>G
NM_005566.3:c.862T>G	NP_005557.1:p.Phe288Val
NR_028500.1:n.1016T>G
NM_005566.4:c.862T>G MANE Select	NP_005557.1:p.Phe288Val
NM_001165415.2:c.688-95T>G	NP_001158887.1:n.688-95T>G
NM_001135239.2:c.688T>G	NP_001128711.1:p.Phe230Val
NM_001165414.2:c.949T>G	NP_001158886.1:p.Phe317Val
NM_001165416.2:c.*12T>G	NP_001158888.1:n.*12T>G
NR_028500.2:n.842T>G