Canonical Allele Identifier: CA2579566226
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19351403del , CM000685.2:g.19351403del GRCh38
NC_000023.10:g.19369521del , CM000685.1:g.19369521del GRCh37
NC_000023.9:g.19279442del NCBI36
NG_016781.1:g.12511del

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.435del ENSP00000348062.6:p.Thr146GlnfsTer?
ENST00000379805.4:c.414del ENSP00000369133.3:p.Thr139GlnfsTer?
ENST00000417819.6:c.498del ENSP00000404616.2:p.Thr167GlnfsTer?
ENST00000423505.6:c.528del ENSP00000406473.2:p.Thr177GlnfsTer?
ENST00000696704.1:c.414del ENSP00000512823.1:p.Thr139GlnfsTer?
ENST00000696705.1:c.414del ENSP00000512824.1:p.Thr139GlnfsTer?
ENST00000422285.7:c.414del MANE Select ENSP00000394382.2:p.Thr139GlnfsTer?
ENST00000355808.9:c.435del ENSP00000348062.5:p.Thr146GlnfsTer?
ENST00000379805.3:c.414del ENSP00000369133.3:p.Thr139GlnfsTer?
ENST00000379806.9:c.528del ENSP00000369134.5:p.Thr177GlnfsTer?
ENST00000422285.6:c.414del ENSP00000394382.2:p.Thr139GlnfsTer?
ENST00000423505.5:c.528del ENSP00000406473.1:p.Thr177GlnfsTer?
ENST00000492364.1:n.516del
ENST00000540249.5:c.414del ENSP00000440761.1:p.Thr139GlnfsTer?
ENST00000545074.5:c.435del ENSP00000438550.1:p.Thr146GlnfsTer?
NM_000284.3:c.414del NP_000275.1:p.Thr139GlnfsTer?
NM_001173454.1:c.528del NP_001166925.1:p.Thr177GlnfsTer?
NM_001173455.1:c.435del NP_001166926.1:p.Thr146GlnfsTer?
NM_001173456.1:c.414del NP_001166927.1:p.Thr139GlnfsTer?
XM_011545531.1:c.549del XP_011543833.1:p.Thr184GlnfsTer?
XM_011545532.1:c.549del XP_011543834.1:p.Thr184GlnfsTer?
XM_017029574.2:c.528del XP_016885063.1:p.Thr177GlnfsTer?
NM_000284.4:c.414del MANE Select NP_000275.1:p.Thr139GlnfsTer?
NM_001173454.2:c.528del NP_001166925.1:p.Thr177GlnfsTer?
NM_001173455.2:c.435del NP_001166926.1:p.Thr146GlnfsTer?
NM_001173456.2:c.414del NP_001166927.1:p.Thr139GlnfsTer?