Canonical Allele Identifier: CA5911451

Gene: LDHA

Linked Data

• dbSNP Id: rs766641807
• ExAC: 11:18428822 A / G
• gnomAD v2: 11-18428822-A-G
• gnomAD v4: 11-18407275-A-G
• MyVariant Identifiers: chr11:g.18428822A>G (hg19) ; chr11:g.18407275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407275A>G , CM000673.2:g.18407275A>G	GRCh38
NC_000011.9:g.18428822A>G , CM000673.1:g.18428822A>G	GRCh37
NC_000011.8:g.18385398A>G	NCBI36
NG_008185.1:g.17841A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.993A>G MANE Select	ENSP00000395337.3:p.Gln331=
ENST00000227157.8:c.*143A>G	ENSP00000227157.4:n.*143A>G
ENST00000375710.7:n.1860A>G
ENST00000379412.9:c.993A>G	ENSP00000368722.5:p.Gln331=
ENST00000396222.6:c.724A>G	ENSP00000379524.2:p.Ile242Val
ENST00000422447.7:c.993A>G	ENSP00000395337.3:p.Gln331=
ENST00000430553.6:c.819A>G	ENSP00000406172.2:p.Gln273=
ENST00000538451.1:n.880A>G
ENST00000540430.5:c.1080A>G	ENSP00000445175.1:p.Gln360=
ENST00000542179.1:c.993A>G	ENSP00000445331.1:p.Gln331=
ENST00000545215.5:c.*737A>G	ENSP00000442637.1:n.*737A>G
NM_001135239.1:c.819A>G	NP_001128711.1:p.Gln273=
NM_001165414.1:c.1080A>G	NP_001158886.1:p.Gln360=
NM_001165415.1:c.724A>G	NP_001158887.1:p.Ile242Val
NM_001165416.1:c.*143A>G	NP_001158888.1:n.*143A>G
NM_005566.3:c.993A>G	NP_005557.1:p.Gln331=
NR_028500.1:n.1147A>G
NM_005566.4:c.993A>G MANE Select	NP_005557.1:p.Gln331=
NM_001165415.2:c.724A>G	NP_001158887.1:p.Ile242Val
NM_001135239.2:c.819A>G	NP_001128711.1:p.Gln273=
NM_001165414.2:c.1080A>G	NP_001158886.1:p.Gln360=
NM_001165416.2:c.*143A>G	NP_001158888.1:n.*143A>G
NR_028500.2:n.973A>G