Canonical Allele Identifier: CA379509852

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428870A>T (hg19) ; chr11:g.18407323A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407323A>T , CM000673.2:g.18407323A>T	GRCh38
NC_000011.9:g.18428870A>T , CM000673.1:g.18428870A>T	GRCh37
NC_000011.8:g.18385446A>T	NCBI36
NG_008185.1:g.17889A>T
NG_011816.1:g.18A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*42A>T MANE Select	ENSP00000395337.3:n.*42A>T
ENST00000227157.8:c.*191A>T	ENSP00000227157.4:n.*191A>T
ENST00000375710.7:n.1908A>T
ENST00000379412.9:c.*42A>T	ENSP00000368722.5:n.*42A>T
ENST00000396222.6:c.772A>T	ENSP00000379524.2:p.Arg258Trp
ENST00000422447.7:c.*42A>T	ENSP00000395337.3:n.*42A>T
ENST00000430553.6:c.*42A>T	ENSP00000406172.2:n.*42A>T
ENST00000538451.1:n.928A>T
ENST00000540430.5:c.*42A>T	ENSP00000445175.1:n.*42A>T
ENST00000545215.5:c.*785A>T	ENSP00000442637.1:n.*785A>T
NM_001135239.1:c.*42A>T	NP_001128711.1:n.*42A>T
NM_001165414.1:c.*42A>T	NP_001158886.1:n.*42A>T
NM_001165415.1:c.772A>T	NP_001158887.1:p.Arg258Trp
NM_001165416.1:c.*191A>T	NP_001158888.1:n.*191A>T
NM_005566.3:c.*42A>T	NP_005557.1:n.*42A>T
NR_028500.1:n.1195A>T
NM_005566.4:c.*42A>T MANE Select	NP_005557.1:n.*42A>T
NM_001165415.2:c.772A>T	NP_001158887.1:p.Arg258Trp
NM_001135239.2:c.*42A>T	NP_001128711.1:n.*42A>T
NM_001165414.2:c.*42A>T	NP_001158886.1:n.*42A>T
NM_001165416.2:c.*191A>T	NP_001158888.1:n.*191A>T
NR_028500.2:n.1021A>T