Canonical Allele Identifier: CA1955586632

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407288C= , CM000673.2:g.18407288C=	GRCh38
NC_000011.9:g.18428835C= , CM000673.1:g.18428835C=	GRCh37
NC_000011.8:g.18385411C=	NCBI36
NG_008185.1:g.17854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*7C= MANE Select	ENSP00000395337.3:n.*7C=
ENST00000227157.8:c.*156C=	ENSP00000227157.4:n.*156C=
ENST00000375710.7:n.1873C=
ENST00000379412.9:c.*7C=	ENSP00000368722.5:n.*7C=
ENST00000396222.6:c.737C=	ENSP00000379524.2:p.Ser246=
ENST00000422447.7:c.*7C=	ENSP00000395337.3:n.*7C=
ENST00000430553.6:c.*7C=	ENSP00000406172.2:n.*7C=
ENST00000538451.1:n.893C=
ENST00000540430.5:c.*7C=	ENSP00000445175.1:n.*7C=
ENST00000545215.5:c.*750C=	ENSP00000442637.1:n.*750C=
NM_001135239.1:c.*7C=	NP_001128711.1:n.*7C=
NM_001165414.1:c.*7C=	NP_001158886.1:n.*7C=
NM_001165415.1:c.737C=	NP_001158887.1:p.Ser246=
NM_001165416.1:c.*156C=	NP_001158888.1:n.*156C=
NM_005566.3:c.*7C=	NP_005557.1:n.*7C=
NR_028500.1:n.1160C=
NM_005566.4:c.*7C= MANE Select	NP_005557.1:n.*7C=
NM_001165415.2:c.737C=	NP_001158887.1:p.Ser246=
NM_001135239.2:c.*7C=	NP_001128711.1:n.*7C=
NM_001165414.2:c.*7C=	NP_001158886.1:n.*7C=
NM_001165416.2:c.*156C=	NP_001158888.1:n.*156C=
NR_028500.2:n.986C=