Canonical Allele Identifier: CA379509868

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428872G>C (hg19) ; chr11:g.18407325G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407325G>C , CM000673.2:g.18407325G>C	GRCh38
NC_000011.9:g.18428872G>C , CM000673.1:g.18428872G>C	GRCh37
NC_000011.8:g.18385448G>C	NCBI36
NG_008185.1:g.17891G>C
NG_011816.1:g.20G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*44G>C MANE Select	ENSP00000395337.3:n.*44G>C
ENST00000227157.8:c.*193G>C	ENSP00000227157.4:n.*193G>C
ENST00000375710.7:n.1910G>C
ENST00000379412.9:c.*44G>C	ENSP00000368722.5:n.*44G>C
ENST00000396222.6:c.774G>C	ENSP00000379524.2:p.Arg258Ser
ENST00000422447.7:c.*44G>C	ENSP00000395337.3:n.*44G>C
ENST00000430553.6:c.*44G>C	ENSP00000406172.2:n.*44G>C
ENST00000538451.1:n.930G>C
ENST00000540430.5:c.*44G>C	ENSP00000445175.1:n.*44G>C
ENST00000545215.5:c.*787G>C	ENSP00000442637.1:n.*787G>C
NM_001135239.1:c.*44G>C	NP_001128711.1:n.*44G>C
NM_001165414.1:c.*44G>C	NP_001158886.1:n.*44G>C
NM_001165415.1:c.774G>C	NP_001158887.1:p.Arg258Ser
NM_001165416.1:c.*193G>C	NP_001158888.1:n.*193G>C
NM_005566.3:c.*44G>C	NP_005557.1:n.*44G>C
NR_028500.1:n.1197G>C
NM_005566.4:c.*44G>C MANE Select	NP_005557.1:n.*44G>C
NM_001165415.2:c.774G>C	NP_001158887.1:p.Arg258Ser
NM_001135239.2:c.*44G>C	NP_001128711.1:n.*44G>C
NM_001165414.2:c.*44G>C	NP_001158886.1:n.*44G>C
NM_001165416.2:c.*193G>C	NP_001158888.1:n.*193G>C
NR_028500.2:n.1023G>C