Canonical Allele Identifier: CA2418222096
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19351291G= , CM000685.2:g.19351291G= GRCh38
NC_000023.10:g.19369409G= , CM000685.1:g.19369409G= GRCh37
NC_000023.9:g.19279330G= NCBI36
NG_016781.1:g.12399G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.323G= ENSP00000348062.6:p.Cys108=
ENST00000379805.4:c.302G= ENSP00000369133.3:p.Cys101=
ENST00000417819.6:c.386G= ENSP00000404616.2:p.Cys129=
ENST00000423505.6:c.416G= ENSP00000406473.2:p.Cys139=
ENST00000696704.1:c.302G= ENSP00000512823.1:p.Cys101=
ENST00000696705.1:c.302G= ENSP00000512824.1:p.Cys101=
ENST00000422285.7:c.302G= MANE Select ENSP00000394382.2:p.Cys101=
ENST00000355808.9:c.323G= ENSP00000348062.5:p.Cys108=
ENST00000379805.3:c.302G= ENSP00000369133.3:p.Cys101=
ENST00000379806.9:c.416G= ENSP00000369134.5:p.Cys139=
ENST00000422285.6:c.302G= ENSP00000394382.2:p.Cys101=
ENST00000423505.5:c.416G= ENSP00000406473.1:p.Cys139=
ENST00000492364.1:n.404G=
ENST00000540249.5:c.302G= ENSP00000440761.1:p.Cys101=
ENST00000545074.5:c.323G= ENSP00000438550.1:p.Cys108=
NM_000284.3:c.302G= NP_000275.1:p.Cys101=
NM_001173454.1:c.416G= NP_001166925.1:p.Cys139=
NM_001173455.1:c.323G= NP_001166926.1:p.Cys108=
NM_001173456.1:c.302G= NP_001166927.1:p.Cys101=
XM_011545531.1:c.437G= XP_011543833.1:p.Cys146=
XM_011545532.1:c.437G= XP_011543834.1:p.Cys146=
XM_017029574.2:c.416G= XP_016885063.1:p.Cys139=
NM_000284.4:c.302G= MANE Select NP_000275.1:p.Cys101=
NM_001173454.2:c.416G= NP_001166925.1:p.Cys139=
NM_001173455.2:c.323G= NP_001166926.1:p.Cys108=
NM_001173456.2:c.302G= NP_001166927.1:p.Cys101=