Canonical Allele Identifier: CA379508802

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428719A>C (hg19) ; chr11:g.18407172A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407172A>C , CM000673.2:g.18407172A>C	GRCh38
NC_000011.9:g.18428719A>C , CM000673.1:g.18428719A>C	GRCh37
NC_000011.8:g.18385295A>C	NCBI36
NG_008185.1:g.17738A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000422447.8:c.890A>C MANE Select	ENSP00000395337.3:p.Gln297Pro
ENST00000227157.8:c.*40A>C	ENSP00000227157.4:n.*40A>C
ENST00000375710.7:n.1757A>C
ENST00000379412.9:c.890A>C	ENSP00000368722.5:p.Gln297Pro
ENST00000396222.6:c.688-67A>C	ENSP00000379524.2:n.688-67A>C
ENST00000422447.7:c.890A>C	ENSP00000395337.3:p.Gln297Pro
ENST00000430553.6:c.716A>C	ENSP00000406172.2:p.Gln239Pro
ENST00000538451.1:n.777A>C
ENST00000540430.5:c.977A>C	ENSP00000445175.1:p.Gln326Pro
ENST00000542179.1:c.890A>C	ENSP00000445331.1:p.Gln297Pro
ENST00000545215.5:c.*634A>C	ENSP00000442637.1:n.*634A>C
NM_001135239.1:c.716A>C	NP_001128711.1:p.Gln239Pro
NM_001165414.1:c.977A>C	NP_001158886.1:p.Gln326Pro
NM_001165415.1:c.688-67A>C	NP_001158887.1:n.688-67A>C
NM_001165416.1:c.*40A>C	NP_001158888.1:n.*40A>C
NM_005566.3:c.890A>C	NP_005557.1:p.Gln297Pro
NR_028500.1:n.1044A>C
NM_005566.4:c.890A>C MANE Select	NP_005557.1:p.Gln297Pro
NM_001165415.2:c.688-67A>C	NP_001158887.1:n.688-67A>C
NM_001135239.2:c.716A>C	NP_001128711.1:p.Gln239Pro
NM_001165414.2:c.977A>C	NP_001158886.1:p.Gln326Pro
NM_001165416.2:c.*40A>C	NP_001158888.1:n.*40A>C
NR_028500.2:n.870A>C