Canonical Allele Identifier: CA473523906

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428774T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407227T>G , CM000673.2:g.18407227T>G	GRCh38
NC_000011.9:g.18428774T>G , CM000673.1:g.18428774T>G	GRCh37
NC_000011.8:g.18385350T>G	NCBI36
NG_008185.1:g.17793T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.945T>G MANE Select	ENSP00000395337.3:p.Arg315=
ENST00000227157.8:c.*95T>G	ENSP00000227157.4:n.*95T>G
ENST00000375710.7:n.1812T>G
ENST00000379412.9:c.945T>G	ENSP00000368722.5:p.Arg315=
ENST00000396222.6:c.688-12T>G	ENSP00000379524.2:n.688-12T>G
ENST00000422447.7:c.945T>G	ENSP00000395337.3:p.Arg315=
ENST00000430553.6:c.771T>G	ENSP00000406172.2:p.Arg257=
ENST00000538451.1:n.832T>G
ENST00000540430.5:c.1032T>G	ENSP00000445175.1:p.Arg344=
ENST00000542179.1:c.945T>G	ENSP00000445331.1:p.Arg315=
ENST00000545215.5:c.*689T>G	ENSP00000442637.1:n.*689T>G
NM_001135239.1:c.771T>G	NP_001128711.1:p.Arg257=
NM_001165414.1:c.1032T>G	NP_001158886.1:p.Arg344=
NM_001165415.1:c.688-12T>G	NP_001158887.1:n.688-12T>G
NM_001165416.1:c.*95T>G	NP_001158888.1:n.*95T>G
NM_005566.3:c.945T>G	NP_005557.1:p.Arg315=
NR_028500.1:n.1099T>G
NM_005566.4:c.945T>G MANE Select	NP_005557.1:p.Arg315=
NM_001165415.2:c.688-12T>G	NP_001158887.1:n.688-12T>G
NM_001135239.2:c.771T>G	NP_001128711.1:p.Arg257=
NM_001165414.2:c.1032T>G	NP_001158886.1:p.Arg344=
NM_001165416.2:c.*95T>G	NP_001158888.1:n.*95T>G
NR_028500.2:n.925T>G