Canonical Allele Identifier: CA379509747

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407309-G-T
• MyVariant Identifiers: chr11:g.18428856G>T (hg19) ; chr11:g.18407309G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407309G>T , CM000673.2:g.18407309G>T	GRCh38
NC_000011.9:g.18428856G>T , CM000673.1:g.18428856G>T	GRCh37
NC_000011.8:g.18385432G>T	NCBI36
NG_008185.1:g.17875G>T
NG_011816.1:g.4G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*28G>T MANE Select	ENSP00000395337.3:n.*28G>T
ENST00000227157.8:c.*177G>T	ENSP00000227157.4:n.*177G>T
ENST00000375710.7:n.1894G>T
ENST00000379412.9:c.*28G>T	ENSP00000368722.5:n.*28G>T
ENST00000396222.6:c.758G>T	ENSP00000379524.2:p.Cys253Phe
ENST00000422447.7:c.*28G>T	ENSP00000395337.3:n.*28G>T
ENST00000430553.6:c.*28G>T	ENSP00000406172.2:n.*28G>T
ENST00000538451.1:n.914G>T
ENST00000540430.5:c.*28G>T	ENSP00000445175.1:n.*28G>T
ENST00000545215.5:c.*771G>T	ENSP00000442637.1:n.*771G>T
NM_001135239.1:c.*28G>T	NP_001128711.1:n.*28G>T
NM_001165414.1:c.*28G>T	NP_001158886.1:n.*28G>T
NM_001165415.1:c.758G>T	NP_001158887.1:p.Cys253Phe
NM_001165416.1:c.*177G>T	NP_001158888.1:n.*177G>T
NM_005566.3:c.*28G>T	NP_005557.1:n.*28G>T
NR_028500.1:n.1181G>T
NM_005566.4:c.*28G>T MANE Select	NP_005557.1:n.*28G>T
NM_001165415.2:c.758G>T	NP_001158887.1:p.Cys253Phe
NM_001135239.2:c.*28G>T	NP_001128711.1:n.*28G>T
NM_001165414.2:c.*28G>T	NP_001158886.1:n.*28G>T
NM_001165416.2:c.*177G>T	NP_001158888.1:n.*177G>T
NR_028500.2:n.1007G>T