Canonical Allele Identifier: CA1955586693
Gene: LDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407404A= , CM000673.2:g.18407404A= GRCh38
NC_000011.9:g.18428951A= , CM000673.1:g.18428951A= GRCh37
NC_000011.8:g.18385527A= NCBI36
NG_008185.1:g.17970A=
NG_011816.1:g.99A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*123A= MANE Select ENSP00000395337.3:n.*123A=
ENST00000227157.8:c.*272A= ENSP00000227157.4:n.*272A=
ENST00000375710.7:n.1989A=
ENST00000379412.9:c.*123A= ENSP00000368722.5:n.*123A=
ENST00000396222.6:c.*28A= ENSP00000379524.2:n.*28A=
ENST00000422447.7:c.*123A= ENSP00000395337.3:n.*123A=
ENST00000430553.6:c.*123A= ENSP00000406172.2:n.*123A=
ENST00000538451.1:n.1009A=
ENST00000540430.5:c.*123A= ENSP00000445175.1:n.*123A=
ENST00000545215.5:c.*866A= ENSP00000442637.1:n.*866A=
NM_001135239.1:c.*123A= NP_001128711.1:n.*123A=
NM_001165414.1:c.*123A= NP_001158886.1:n.*123A=
NM_001165415.1:c.*28A= NP_001158887.1:n.*28A=
NM_001165416.1:c.*272A= NP_001158888.1:n.*272A=
NM_005566.3:c.*123A= NP_005557.1:n.*123A=
NR_028500.1:n.1276A=
NM_005566.4:c.*123A= MANE Select NP_005557.1:n.*123A=
NM_001165415.2:c.*28A= NP_001158887.1:n.*28A=
NM_001135239.2:c.*123A= NP_001128711.1:n.*123A=
NM_001165414.2:c.*123A= NP_001158886.1:n.*123A=
NM_001165416.2:c.*272A= NP_001158888.1:n.*272A=
NR_028500.2:n.1102A=