Canonical Allele Identifier: CA379510438

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428917T>G (hg19) ; chr11:g.18407370T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407370T>G , CM000673.2:g.18407370T>G	GRCh38
NC_000011.9:g.18428917T>G , CM000673.1:g.18428917T>G	GRCh37
NC_000011.8:g.18385493T>G	NCBI36
NG_008185.1:g.17936T>G
NG_011816.1:g.65T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*89T>G MANE Select	ENSP00000395337.3:n.*89T>G
ENST00000227157.8:c.*238T>G	ENSP00000227157.4:n.*238T>G
ENST00000375710.7:n.1955T>G
ENST00000379412.9:c.*89T>G	ENSP00000368722.5:n.*89T>G
ENST00000396222.6:c.819T>G	ENSP00000379524.2:p.Cys273Trp
ENST00000422447.7:c.*89T>G	ENSP00000395337.3:n.*89T>G
ENST00000430553.6:c.*89T>G	ENSP00000406172.2:n.*89T>G
ENST00000538451.1:n.975T>G
ENST00000540430.5:c.*89T>G	ENSP00000445175.1:n.*89T>G
ENST00000545215.5:c.*832T>G	ENSP00000442637.1:n.*832T>G
NM_001135239.1:c.*89T>G	NP_001128711.1:n.*89T>G
NM_001165414.1:c.*89T>G	NP_001158886.1:n.*89T>G
NM_001165415.1:c.819T>G	NP_001158887.1:p.Cys273Trp
NM_001165416.1:c.*238T>G	NP_001158888.1:n.*238T>G
NM_005566.3:c.*89T>G	NP_005557.1:n.*89T>G
NR_028500.1:n.1242T>G
NM_005566.4:c.*89T>G MANE Select	NP_005557.1:n.*89T>G
NM_001165415.2:c.819T>G	NP_001158887.1:p.Cys273Trp
NM_001135239.2:c.*89T>G	NP_001128711.1:n.*89T>G
NM_001165414.2:c.*89T>G	NP_001158886.1:n.*89T>G
NM_001165416.2:c.*238T>G	NP_001158888.1:n.*238T>G
NR_028500.2:n.1068T>G