Canonical Allele Identifier: CA1955586585

Gene: LDHA

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.875C= MANE Select	ENSP00000395337.3:p.Pro292=
ENST00000227157.8:c.*25C=	ENSP00000227157.4:n.*25C=
ENST00000375710.7:n.1742C=
ENST00000379412.9:c.875C=	ENSP00000368722.5:p.Pro292=
ENST00000396222.6:c.688-82C=	ENSP00000379524.2:n.688-82C=
ENST00000422447.7:c.875C=	ENSP00000395337.3:p.Pro292=
ENST00000430553.6:c.701C=	ENSP00000406172.2:p.Pro234=
ENST00000538451.1:n.762C=
ENST00000540430.5:c.962C=	ENSP00000445175.1:p.Pro321=
ENST00000541097.5:c.*213C=	ENSP00000443362.1:n.*213C=
ENST00000542179.1:c.875C=	ENSP00000445331.1:p.Pro292=
ENST00000545215.5:c.*619C=	ENSP00000442637.1:n.*619C=
NM_001135239.1:c.701C=	NP_001128711.1:p.Pro234=
NM_001165414.1:c.962C=	NP_001158886.1:p.Pro321=
NM_001165415.1:c.688-82C=	NP_001158887.1:n.688-82C=
NM_001165416.1:c.*25C=	NP_001158888.1:n.*25C=
NM_005566.3:c.875C=	NP_005557.1:p.Pro292=
NR_028500.1:n.1029C=
NM_005566.4:c.875C= MANE Select	NP_005557.1:p.Pro292=
NM_001165415.2:c.688-82C=	NP_001158887.1:n.688-82C=
NM_001135239.2:c.701C=	NP_001128711.1:p.Pro234=
NM_001165414.2:c.962C=	NP_001158886.1:p.Pro321=
NM_001165416.2:c.*25C=	NP_001158888.1:n.*25C=
NR_028500.2:n.855C=