Canonical Allele Identifier: CA1955586703

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407433A= , CM000673.2:g.18407433A=	GRCh38
NC_000011.9:g.18428980A= , CM000673.1:g.18428980A=	GRCh37
NC_000011.8:g.18385556A=	NCBI36
NG_008185.1:g.17999A=
NG_011816.1:g.128A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*152A= MANE Select	ENSP00000395337.3:n.*152A=
ENST00000227157.8:c.*301A=	ENSP00000227157.4:n.*301A=
ENST00000375710.7:n.2018A=
ENST00000379412.9:c.*152A=	ENSP00000368722.5:n.*152A=
ENST00000396222.6:c.*57A=	ENSP00000379524.2:n.*57A=
ENST00000422447.7:c.*152A=	ENSP00000395337.3:n.*152A=
ENST00000430553.6:c.*152A=	ENSP00000406172.2:n.*152A=
ENST00000538451.1:n.1038A=
ENST00000540430.5:c.*152A=	ENSP00000445175.1:n.*152A=
ENST00000545215.5:c.*895A=	ENSP00000442637.1:n.*895A=
NM_001135239.1:c.*152A=	NP_001128711.1:n.*152A=
NM_001165414.1:c.*152A=	NP_001158886.1:n.*152A=
NM_001165415.1:c.*57A=	NP_001158887.1:n.*57A=
NM_001165416.1:c.*301A=	NP_001158888.1:n.*301A=
NM_005566.3:c.*152A=	NP_005557.1:n.*152A=
NR_028500.1:n.1305A=
NM_005566.4:c.*152A= MANE Select	NP_005557.1:n.*152A=
NM_001165415.2:c.*57A=	NP_001158887.1:n.*57A=
NM_001135239.2:c.*152A=	NP_001128711.1:n.*152A=
NM_001165414.2:c.*152A=	NP_001158886.1:n.*152A=
NM_001165416.2:c.*301A=	NP_001158888.1:n.*301A=
NR_028500.2:n.1131A=