Canonical Allele Identifier: CA379508799

Gene: LDHA

Linked Data

• COSMIC: COSM2155071 ; COSM2155072
• MyVariant Identifiers: chr11:g.18428718C>T (hg19) ; chr11:g.18407171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407171C>T , CM000673.2:g.18407171C>T	GRCh38
NC_000011.9:g.18428718C>T , CM000673.1:g.18428718C>T	GRCh37
NC_000011.8:g.18385294C>T	NCBI36
NG_008185.1:g.17737C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000422447.8:c.889C>T MANE Select	ENSP00000395337.3:p.Gln297Ter
ENST00000227157.8:c.*39C>T	ENSP00000227157.4:n.*39C>T
ENST00000375710.7:n.1756C>T
ENST00000379412.9:c.889C>T	ENSP00000368722.5:p.Gln297Ter
ENST00000396222.6:c.688-68C>T	ENSP00000379524.2:n.688-68C>T
ENST00000422447.7:c.889C>T	ENSP00000395337.3:p.Gln297Ter
ENST00000430553.6:c.715C>T	ENSP00000406172.2:p.Gln239Ter
ENST00000538451.1:n.776C>T
ENST00000540430.5:c.976C>T	ENSP00000445175.1:p.Gln326Ter
ENST00000542179.1:c.889C>T	ENSP00000445331.1:p.Gln297Ter
ENST00000545215.5:c.*633C>T	ENSP00000442637.1:n.*633C>T
NM_001135239.1:c.715C>T	NP_001128711.1:p.Gln239Ter
NM_001165414.1:c.976C>T	NP_001158886.1:p.Gln326Ter
NM_001165415.1:c.688-68C>T	NP_001158887.1:n.688-68C>T
NM_001165416.1:c.*39C>T	NP_001158888.1:n.*39C>T
NM_005566.3:c.889C>T	NP_005557.1:p.Gln297Ter
NR_028500.1:n.1043C>T
NM_005566.4:c.889C>T MANE Select	NP_005557.1:p.Gln297Ter
NM_001165415.2:c.688-68C>T	NP_001158887.1:n.688-68C>T
NM_001135239.2:c.715C>T	NP_001128711.1:p.Gln239Ter
NM_001165414.2:c.976C>T	NP_001158886.1:p.Gln326Ter
NM_001165416.2:c.*39C>T	NP_001158888.1:n.*39C>T
NR_028500.2:n.869C>T