Canonical Allele Identifier: CA379509397

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428821A>C (hg19) ; chr11:g.18407274A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407274A>C , CM000673.2:g.18407274A>C	GRCh38
NC_000011.9:g.18428821A>C , CM000673.1:g.18428821A>C	GRCh37
NC_000011.8:g.18385397A>C	NCBI36
NG_008185.1:g.17840A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.992A>C MANE Select	ENSP00000395337.3:p.Gln331Pro
ENST00000227157.8:c.*142A>C	ENSP00000227157.4:n.*142A>C
ENST00000375710.7:n.1859A>C
ENST00000379412.9:c.992A>C	ENSP00000368722.5:p.Gln331Pro
ENST00000396222.6:c.723A>C	ENSP00000379524.2:p.Ala241=
ENST00000422447.7:c.992A>C	ENSP00000395337.3:p.Gln331Pro
ENST00000430553.6:c.818A>C	ENSP00000406172.2:p.Gln273Pro
ENST00000538451.1:n.879A>C
ENST00000540430.5:c.1079A>C	ENSP00000445175.1:p.Gln360Pro
ENST00000542179.1:c.992A>C	ENSP00000445331.1:p.Gln331Pro
ENST00000545215.5:c.*736A>C	ENSP00000442637.1:n.*736A>C
NM_001135239.1:c.818A>C	NP_001128711.1:p.Gln273Pro
NM_001165414.1:c.1079A>C	NP_001158886.1:p.Gln360Pro
NM_001165415.1:c.723A>C	NP_001158887.1:p.Ala241=
NM_001165416.1:c.*142A>C	NP_001158888.1:n.*142A>C
NM_005566.3:c.992A>C	NP_005557.1:p.Gln331Pro
NR_028500.1:n.1146A>C
NM_005566.4:c.992A>C MANE Select	NP_005557.1:p.Gln331Pro
NM_001165415.2:c.723A>C	NP_001158887.1:p.Ala241=
NM_001135239.2:c.818A>C	NP_001128711.1:p.Gln273Pro
NM_001165414.2:c.1079A>C	NP_001158886.1:p.Gln360Pro
NM_001165416.2:c.*142A>C	NP_001158888.1:n.*142A>C
NR_028500.2:n.972A>C