Canonical Allele Identifier: CA597491497

Gene: LDHA

Linked Data

• dbSNP Id: rs1487370116
• gnomAD v2: 11-18428998-C-T
• MyVariant Identifiers: chr11:g.18428998C>T (hg19) ; chr11:g.18407451C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407451C>T , CM000673.2:g.18407451C>T	GRCh38
NC_000011.9:g.18428998C>T , CM000673.1:g.18428998C>T	GRCh37
NC_000011.8:g.18385574C>T	NCBI36
NG_008185.1:g.18017C>T
NG_011816.1:g.146C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*170C>T MANE Select	ENSP00000395337.3:n.*170C>T
ENST00000227157.8:c.*319C>T	ENSP00000227157.4:n.*319C>T
ENST00000375710.7:n.2036C>T
ENST00000379412.9:c.*170C>T	ENSP00000368722.5:n.*170C>T
ENST00000396222.6:c.*75C>T	ENSP00000379524.2:n.*75C>T
ENST00000422447.7:c.*170C>T	ENSP00000395337.3:n.*170C>T
ENST00000430553.6:c.*170C>T	ENSP00000406172.2:n.*170C>T
ENST00000538451.1:n.1056C>T
ENST00000540430.5:c.*170C>T	ENSP00000445175.1:n.*170C>T
ENST00000545215.5:c.*913C>T	ENSP00000442637.1:n.*913C>T
NM_001135239.1:c.*170C>T	NP_001128711.1:n.*170C>T
NM_001165414.1:c.*170C>T	NP_001158886.1:n.*170C>T
NM_001165415.1:c.*75C>T	NP_001158887.1:n.*75C>T
NM_001165416.1:c.*319C>T	NP_001158888.1:n.*319C>T
NM_005566.3:c.*170C>T	NP_005557.1:n.*170C>T
NR_028500.1:n.1323C>T
NM_005566.4:c.*170C>T MANE Select	NP_005557.1:n.*170C>T
NM_001165415.2:c.*75C>T	NP_001158887.1:n.*75C>T
NM_001135239.2:c.*170C>T	NP_001128711.1:n.*170C>T
NM_001165414.2:c.*170C>T	NP_001158886.1:n.*170C>T
NM_001165416.2:c.*319C>T	NP_001158888.1:n.*319C>T
NR_028500.2:n.1149C>T