Canonical Allele Identifier: CA2418224608
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19357659T= , CM000685.2:g.19357659T= GRCh38
NC_000023.10:g.19375777T= , CM000685.1:g.19375777T= GRCh37
NC_000023.9:g.19285698T= NCBI36
NG_016781.1:g.18767T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.860T= ENSP00000348062.6:p.Ile287=
ENST00000379805.4:c.*531T= ENSP00000369133.3:n.*531T=
ENST00000417819.6:c.923T= ENSP00000404616.2:p.Ile308=
ENST00000423505.6:c.953T= ENSP00000406473.2:p.Ile318=
ENST00000481733.2:n.634T=
ENST00000696704.1:c.*171T= ENSP00000512823.1:n.*171T=
ENST00000696705.1:c.*294T= ENSP00000512824.1:n.*294T=
ENST00000422285.7:c.839T= MANE Select ENSP00000394382.2:p.Ile280=
ENST00000379804.1:c.-5T= ENSP00000369132.1:n.-5T=
ENST00000379806.9:c.953T= ENSP00000369134.5:p.Ile318=
ENST00000422285.6:c.839T= ENSP00000394382.2:p.Ile280=
ENST00000478795.1:n.278T=
ENST00000481733.1:n.267T=
ENST00000540249.5:c.746T= ENSP00000440761.1:p.Ile249=
ENST00000545074.5:c.860T= ENSP00000438550.1:p.Ile287=
NM_000284.3:c.839T= NP_000275.1:p.Ile280=
NM_001173454.1:c.953T= NP_001166925.1:p.Ile318=
NM_001173455.1:c.860T= NP_001166926.1:p.Ile287=
NM_001173456.1:c.746T= NP_001166927.1:p.Ile249=
XM_011545531.1:c.974T= XP_011543833.1:p.Ile325=
XM_011545532.1:c.881T= XP_011543834.1:p.Ile294=
XM_017029574.2:c.860T= XP_016885063.1:p.Ile287=
NM_000284.4:c.839T= MANE Select NP_000275.1:p.Ile280=
NM_001173454.2:c.953T= NP_001166925.1:p.Ile318=
NM_001173455.2:c.860T= NP_001166926.1:p.Ile287=
NM_001173456.2:c.746T= NP_001166927.1:p.Ile249=