Canonical Allele Identifier: CA1955586689
Gene: LDHA HGNC NCBI

Linked Data

dbSNP Id: rs1866731252

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18407390del , CM000673.2:g.18407390del GRCh38
NC_000011.9:g.18428937del , CM000673.1:g.18428937del GRCh37
NC_000011.8:g.18385513del NCBI36
NG_008185.1:g.17956del
NG_011816.1:g.85del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422447.8:c.*109del MANE Select ENSP00000395337.3:n.*109del
ENST00000227157.8:c.*258del ENSP00000227157.4:n.*258del
ENST00000375710.7:n.1975del
ENST00000379412.9:c.*109del ENSP00000368722.5:n.*109del
ENST00000396222.6:c.*14del ENSP00000379524.2:n.*14del
ENST00000422447.7:c.*109del ENSP00000395337.3:n.*109del
ENST00000430553.6:c.*109del ENSP00000406172.2:n.*109del
ENST00000538451.1:n.995del
ENST00000540430.5:c.*109del ENSP00000445175.1:n.*109del
ENST00000545215.5:c.*852del ENSP00000442637.1:n.*852del
NM_001135239.1:c.*109del NP_001128711.1:n.*109del
NM_001165414.1:c.*109del NP_001158886.1:n.*109del
NM_001165415.1:c.*14del NP_001158887.1:n.*14del
NM_001165416.1:c.*258del NP_001158888.1:n.*258del
NM_005566.3:c.*109del NP_005557.1:n.*109del
NR_028500.1:n.1262del
NM_005566.4:c.*109del MANE Select NP_005557.1:n.*109del
NM_001165415.2:c.*14del NP_001158887.1:n.*14del
NM_001135239.2:c.*109del NP_001128711.1:n.*109del
NM_001165414.2:c.*109del NP_001158886.1:n.*109del
NM_001165416.2:c.*258del NP_001158888.1:n.*258del
NR_028500.2:n.1088del