Canonical Allele Identifier: CA473523865

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428720G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407173G>A , CM000673.2:g.18407173G>A	GRCh38
NC_000011.9:g.18428720G>A , CM000673.1:g.18428720G>A	GRCh37
NC_000011.8:g.18385296G>A	NCBI36
NG_008185.1:g.17739G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000422447.8:c.891G>A MANE Select	ENSP00000395337.3:p.Gln297=
ENST00000227157.8:c.*41G>A	ENSP00000227157.4:n.*41G>A
ENST00000375710.7:n.1758G>A
ENST00000379412.9:c.891G>A	ENSP00000368722.5:p.Gln297=
ENST00000396222.6:c.688-66G>A	ENSP00000379524.2:n.688-66G>A
ENST00000422447.7:c.891G>A	ENSP00000395337.3:p.Gln297=
ENST00000430553.6:c.717G>A	ENSP00000406172.2:p.Gln239=
ENST00000538451.1:n.778G>A
ENST00000540430.5:c.978G>A	ENSP00000445175.1:p.Gln326=
ENST00000542179.1:c.891G>A	ENSP00000445331.1:p.Gln297=
ENST00000545215.5:c.*635G>A	ENSP00000442637.1:n.*635G>A
NM_001135239.1:c.717G>A	NP_001128711.1:p.Gln239=
NM_001165414.1:c.978G>A	NP_001158886.1:p.Gln326=
NM_001165415.1:c.688-66G>A	NP_001158887.1:n.688-66G>A
NM_001165416.1:c.*41G>A	NP_001158888.1:n.*41G>A
NM_005566.3:c.891G>A	NP_005557.1:p.Gln297=
NR_028500.1:n.1045G>A
NM_005566.4:c.891G>A MANE Select	NP_005557.1:p.Gln297=
NM_001165415.2:c.688-66G>A	NP_001158887.1:n.688-66G>A
NM_001135239.2:c.717G>A	NP_001128711.1:p.Gln239=
NM_001165414.2:c.978G>A	NP_001158886.1:p.Gln326=
NM_001165416.2:c.*41G>A	NP_001158888.1:n.*41G>A
NR_028500.2:n.871G>A