Canonical Allele Identifier: CA1955586591
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407174A= , CM000673.2:g.18407174A= GRCh38
NC_000011.9:g.18428721A= , CM000673.1:g.18428721A= GRCh37
NC_000011.8:g.18385297A= NCBI36
NG_008185.1:g.17740A=

Transcript Alleles

HGVS Amino-acid change
ENST00000422447.8:c.892A= MANE Select ENSP00000395337.3:p.Asn298=
ENST00000227157.8:c.*42A= ENSP00000227157.4:n.*42A=
ENST00000375710.7:n.1759A=
ENST00000379412.9:c.892A= ENSP00000368722.5:p.Asn298=
ENST00000396222.6:c.688-65A= ENSP00000379524.2:n.688-65A=
ENST00000422447.7:c.892A= ENSP00000395337.3:p.Asn298=
ENST00000430553.6:c.718A= ENSP00000406172.2:p.Asn240=
ENST00000538451.1:n.779A=
ENST00000540430.5:c.979A= ENSP00000445175.1:p.Asn327=
ENST00000542179.1:c.892A= ENSP00000445331.1:p.Asn298=
ENST00000545215.5:c.*636A= ENSP00000442637.1:n.*636A=
NM_001135239.1:c.718A= NP_001128711.1:p.Asn240=
NM_001165414.1:c.979A= NP_001158886.1:p.Asn327=
NM_001165415.1:c.688-65A= NP_001158887.1:n.688-65A=
NM_001165416.1:c.*42A= NP_001158888.1:n.*42A=
NM_005566.3:c.892A= NP_005557.1:p.Asn298=
NR_028500.1:n.1046A=
NM_005566.4:c.892A= MANE Select NP_005557.1:p.Asn298=
NM_001165415.2:c.688-65A= NP_001158887.1:n.688-65A=
NM_001135239.2:c.718A= NP_001128711.1:p.Asn240=
NM_001165414.2:c.979A= NP_001158886.1:p.Asn327=
NM_001165416.2:c.*42A= NP_001158888.1:n.*42A=
NR_028500.2:n.872A=