Canonical Allele Identifier: CA379508752

Gene: LDHA

Linked Data

• dbSNP Id: rs1866717274
• gnomAD v4: 11-18407157-C-T
• MyVariant Identifiers: chr11:g.18428704C>T (hg19) ; chr11:g.18407157C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407157C>T , CM000673.2:g.18407157C>T	GRCh38
NC_000011.9:g.18428704C>T , CM000673.1:g.18428704C>T	GRCh37
NC_000011.8:g.18385280C>T	NCBI36
NG_008185.1:g.17723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.875C>T MANE Select	ENSP00000395337.3:p.Pro292Leu
ENST00000227157.8:c.*25C>T	ENSP00000227157.4:n.*25C>T
ENST00000375710.7:n.1742C>T
ENST00000379412.9:c.875C>T	ENSP00000368722.5:p.Pro292Leu
ENST00000396222.6:c.688-82C>T	ENSP00000379524.2:n.688-82C>T
ENST00000422447.7:c.875C>T	ENSP00000395337.3:p.Pro292Leu
ENST00000430553.6:c.701C>T	ENSP00000406172.2:p.Pro234Leu
ENST00000538451.1:n.762C>T
ENST00000540430.5:c.962C>T	ENSP00000445175.1:p.Pro321Leu
ENST00000541097.5:c.*213C>T	ENSP00000443362.1:n.*213C>T
ENST00000542179.1:c.875C>T	ENSP00000445331.1:p.Pro292Leu
ENST00000545215.5:c.*619C>T	ENSP00000442637.1:n.*619C>T
NM_001135239.1:c.701C>T	NP_001128711.1:p.Pro234Leu
NM_001165414.1:c.962C>T	NP_001158886.1:p.Pro321Leu
NM_001165415.1:c.688-82C>T	NP_001158887.1:n.688-82C>T
NM_001165416.1:c.*25C>T	NP_001158888.1:n.*25C>T
NM_005566.3:c.875C>T	NP_005557.1:p.Pro292Leu
NR_028500.1:n.1029C>T
NM_005566.4:c.875C>T MANE Select	NP_005557.1:p.Pro292Leu
NM_001165415.2:c.688-82C>T	NP_001158887.1:n.688-82C>T
NM_001135239.2:c.701C>T	NP_001128711.1:p.Pro234Leu
NM_001165414.2:c.962C>T	NP_001158886.1:p.Pro321Leu
NM_001165416.2:c.*25C>T	NP_001158888.1:n.*25C>T
NR_028500.2:n.855C>T