Canonical Allele Identifier: CA5911457

Gene: LDHA

Linked Data

• dbSNP Id: rs753690566
• ExAC: 11:18428853 A / C
• gnomAD v2: 11-18428853-A-C
• gnomAD v3: 11-18407306-A-C
• gnomAD v4: 11-18407306-A-C
• MyVariant Identifiers: chr11:g.18428853A>C (hg19) ; chr11:g.18407306A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407306A>C , CM000673.2:g.18407306A>C	GRCh38
NC_000011.9:g.18428853A>C , CM000673.1:g.18428853A>C	GRCh37
NC_000011.8:g.18385429A>C	NCBI36
NG_008185.1:g.17872A>C
NG_011816.1:g.1A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*25A>C MANE Select	ENSP00000395337.3:n.*25A>C
ENST00000227157.8:c.*174A>C	ENSP00000227157.4:n.*174A>C
ENST00000375710.7:n.1891A>C
ENST00000379412.9:c.*25A>C	ENSP00000368722.5:n.*25A>C
ENST00000396222.6:c.755A>C	ENSP00000379524.2:p.His252Pro
ENST00000422447.7:c.*25A>C	ENSP00000395337.3:n.*25A>C
ENST00000430553.6:c.*25A>C	ENSP00000406172.2:n.*25A>C
ENST00000538451.1:n.911A>C
ENST00000540430.5:c.*25A>C	ENSP00000445175.1:n.*25A>C
ENST00000545215.5:c.*768A>C	ENSP00000442637.1:n.*768A>C
NM_001135239.1:c.*25A>C	NP_001128711.1:n.*25A>C
NM_001165414.1:c.*25A>C	NP_001158886.1:n.*25A>C
NM_001165415.1:c.755A>C	NP_001158887.1:p.His252Pro
NM_001165416.1:c.*174A>C	NP_001158888.1:n.*174A>C
NM_005566.3:c.*25A>C	NP_005557.1:n.*25A>C
NR_028500.1:n.1178A>C
NM_005566.4:c.*25A>C MANE Select	NP_005557.1:n.*25A>C
NM_001165415.2:c.755A>C	NP_001158887.1:p.His252Pro
NM_001135239.2:c.*25A>C	NP_001128711.1:n.*25A>C
NM_001165414.2:c.*25A>C	NP_001158886.1:n.*25A>C
NM_001165416.2:c.*174A>C	NP_001158888.1:n.*174A>C
NR_028500.2:n.1004A>C