Canonical Allele Identifier: CA379509416

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428823T>A (hg19) ; chr11:g.18407276T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407276T>A , CM000673.2:g.18407276T>A	GRCh38
NC_000011.9:g.18428823T>A , CM000673.1:g.18428823T>A	GRCh37
NC_000011.8:g.18385399T>A	NCBI36
NG_008185.1:g.17842T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.994T>A MANE Select	ENSP00000395337.3:p.Phe332Ile
ENST00000227157.8:c.*144T>A	ENSP00000227157.4:n.*144T>A
ENST00000375710.7:n.1861T>A
ENST00000379412.9:c.994T>A	ENSP00000368722.5:p.Phe332Ile
ENST00000396222.6:c.725T>A	ENSP00000379524.2:p.Ile242Asn
ENST00000422447.7:c.994T>A	ENSP00000395337.3:p.Phe332Ile
ENST00000430553.6:c.820T>A	ENSP00000406172.2:p.Phe274Ile
ENST00000538451.1:n.881T>A
ENST00000540430.5:c.1081T>A	ENSP00000445175.1:p.Phe361Ile
ENST00000542179.1:c.994T>A	ENSP00000445331.1:p.Phe332Ile
ENST00000545215.5:c.*738T>A	ENSP00000442637.1:n.*738T>A
NM_001135239.1:c.820T>A	NP_001128711.1:p.Phe274Ile
NM_001165414.1:c.1081T>A	NP_001158886.1:p.Phe361Ile
NM_001165415.1:c.725T>A	NP_001158887.1:p.Ile242Asn
NM_001165416.1:c.*144T>A	NP_001158888.1:n.*144T>A
NM_005566.3:c.994T>A	NP_005557.1:p.Phe332Ile
NR_028500.1:n.1148T>A
NM_005566.4:c.994T>A MANE Select	NP_005557.1:p.Phe332Ile
NM_001165415.2:c.725T>A	NP_001158887.1:p.Ile242Asn
NM_001135239.2:c.820T>A	NP_001128711.1:p.Phe274Ile
NM_001165414.2:c.1081T>A	NP_001158886.1:p.Phe361Ile
NM_001165416.2:c.*144T>A	NP_001158888.1:n.*144T>A
NR_028500.2:n.974T>A