Canonical Allele Identifier: CA473523870
Gene: LDHA HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.18428729C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407182C>A , CM000673.2:g.18407182C>A GRCh38
NC_000011.9:g.18428729C>A , CM000673.1:g.18428729C>A GRCh37
NC_000011.8:g.18385305C>A NCBI36
NG_008185.1:g.17748C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000422447.8:c.900C>A MANE Select ENSP00000395337.3:p.Ile300=
ENST00000227157.8:c.*50C>A ENSP00000227157.4:n.*50C>A
ENST00000375710.7:n.1767C>A
ENST00000379412.9:c.900C>A ENSP00000368722.5:p.Ile300=
ENST00000396222.6:c.688-57C>A ENSP00000379524.2:n.688-57C>A
ENST00000422447.7:c.900C>A ENSP00000395337.3:p.Ile300=
ENST00000430553.6:c.726C>A ENSP00000406172.2:p.Ile242=
ENST00000538451.1:n.787C>A
ENST00000540430.5:c.987C>A ENSP00000445175.1:p.Ile329=
ENST00000542179.1:c.900C>A ENSP00000445331.1:p.Ile300=
ENST00000545215.5:c.*644C>A ENSP00000442637.1:n.*644C>A
NM_001135239.1:c.726C>A NP_001128711.1:p.Ile242=
NM_001165414.1:c.987C>A NP_001158886.1:p.Ile329=
NM_001165415.1:c.688-57C>A NP_001158887.1:n.688-57C>A
NM_001165416.1:c.*50C>A NP_001158888.1:n.*50C>A
NM_005566.3:c.900C>A NP_005557.1:p.Ile300=
NR_028500.1:n.1054C>A
NM_005566.4:c.900C>A MANE Select NP_005557.1:p.Ile300=
NM_001165415.2:c.688-57C>A NP_001158887.1:n.688-57C>A
NM_001135239.2:c.726C>A NP_001128711.1:p.Ile242=
NM_001165414.2:c.987C>A NP_001158886.1:p.Ile329=
NM_001165416.2:c.*50C>A NP_001158888.1:n.*50C>A
NR_028500.2:n.880C>A