Canonical Allele Identifier: CA1955586611

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407241C= , CM000673.2:g.18407241C=	GRCh38
NC_000011.9:g.18428788C= , CM000673.1:g.18428788C=	GRCh37
NC_000011.8:g.18385364C=	NCBI36
NG_008185.1:g.17807C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.959C= MANE Select	ENSP00000395337.3:p.Ala320=
ENST00000227157.8:c.*109C=	ENSP00000227157.4:n.*109C=
ENST00000375710.7:n.1826C=
ENST00000379412.9:c.959C=	ENSP00000368722.5:p.Ala320=
ENST00000396222.6:c.690C=	ENSP00000379524.2:p.Cys230=
ENST00000422447.7:c.959C=	ENSP00000395337.3:p.Ala320=
ENST00000430553.6:c.785C=	ENSP00000406172.2:p.Ala262=
ENST00000538451.1:n.846C=
ENST00000540430.5:c.1046C=	ENSP00000445175.1:p.Ala349=
ENST00000542179.1:c.959C=	ENSP00000445331.1:p.Ala320=
ENST00000545215.5:c.*703C=	ENSP00000442637.1:n.*703C=
NM_001135239.1:c.785C=	NP_001128711.1:p.Ala262=
NM_001165414.1:c.1046C=	NP_001158886.1:p.Ala349=
NM_001165415.1:c.690C=	NP_001158887.1:p.Cys230=
NM_001165416.1:c.*109C=	NP_001158888.1:n.*109C=
NM_005566.3:c.959C=	NP_005557.1:p.Ala320=
NR_028500.1:n.1113C=
NM_005566.4:c.959C= MANE Select	NP_005557.1:p.Ala320=
NM_001165415.2:c.690C=	NP_001158887.1:p.Cys230=
NM_001135239.2:c.785C=	NP_001128711.1:p.Ala262=
NM_001165414.2:c.1046C=	NP_001158886.1:p.Ala349=
NM_001165416.2:c.*109C=	NP_001158888.1:n.*109C=
NR_028500.2:n.939C=