Canonical Allele Identifier: CA2693250971
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19357819del , CM000685.2:g.19357819del GRCh38
NC_000023.10:g.19375937del , CM000685.1:g.19375937del GRCh37
NC_000023.9:g.19285858del NCBI36
NG_016781.1:g.18927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.920+100del ENSP00000348062.6:n.920+100del
ENST00000379805.4:c.*591+100del ENSP00000369133.3:n.*591+100del
ENST00000417819.6:c.983+100del ENSP00000404616.2:n.983+100del
ENST00000423505.6:c.1013+100del ENSP00000406473.2:n.1013+100del
ENST00000481733.2:n.694+100del
ENST00000696704.1:c.*231+100del ENSP00000512823.1:n.*231+100del
ENST00000696705.1:c.*354+100del ENSP00000512824.1:n.*354+100del
ENST00000422285.7:c.899+100del MANE Select ENSP00000394382.2:n.899+100del
ENST00000379804.1:c.56+100del ENSP00000369132.1:n.56+100del
ENST00000379806.9:c.1013+100del ENSP00000369134.5:n.1013+100del
ENST00000422285.6:c.899+100del ENSP00000394382.2:n.899+100del
ENST00000478795.1:n.338+100del
ENST00000481733.1:n.327+100del
ENST00000540249.5:c.806+100del ENSP00000440761.1:n.806+100del
ENST00000545074.5:c.920+100del ENSP00000438550.1:n.920+100del
NM_000284.3:c.899+100del NP_000275.1:n.899+100del
NM_001173454.1:c.1013+100del NP_001166925.1:n.1013+100del
NM_001173455.1:c.920+100del NP_001166926.1:n.920+100del
NM_001173456.1:c.806+100del NP_001166927.1:n.806+100del
XM_011545531.1:c.1034+100del XP_011543833.1:n.1034+100del
XM_011545532.1:c.941+100del XP_011543834.1:n.941+100del
XM_017029574.2:c.920+100del XP_016885063.1:n.920+100del
NM_000284.4:c.899+100del MANE Select NP_000275.1:n.899+100del
NM_001173454.2:c.1013+100del NP_001166925.1:n.1013+100del
NM_001173455.2:c.920+100del NP_001166926.1:n.920+100del
NM_001173456.2:c.806+100del NP_001166927.1:n.806+100del