Canonical Allele Identifier: CA2418223745
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355701A= , CM000685.2:g.19355701A= GRCh38
NC_000023.10:g.19373819A= , CM000685.1:g.19373819A= GRCh37
NC_000023.9:g.19283740A= NCBI36
NG_016781.1:g.16809A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.796A= ENSP00000348062.6:p.Ile266=
ENST00000379805.4:c.*467A= ENSP00000369133.3:n.*467A=
ENST00000417819.6:c.859A= ENSP00000404616.2:p.Ile287=
ENST00000423505.6:c.889A= ENSP00000406473.2:p.Ile297=
ENST00000481733.2:n.570A=
ENST00000696704.1:c.*107A= ENSP00000512823.1:n.*107A=
ENST00000696705.1:c.*230A= ENSP00000512824.1:n.*230A=
ENST00000422285.7:c.775A= MANE Select ENSP00000394382.2:p.Ile259=
ENST00000379804.1:c.-69A= ENSP00000369132.1:n.-69A=
ENST00000379806.9:c.889A= ENSP00000369134.5:p.Ile297=
ENST00000422285.6:c.775A= ENSP00000394382.2:p.Ile259=
ENST00000481733.1:n.203A=
ENST00000540249.5:c.682A= ENSP00000440761.1:p.Ile228=
ENST00000545074.5:c.796A= ENSP00000438550.1:p.Ile266=
NM_000284.3:c.775A= NP_000275.1:p.Ile259=
NM_001173454.1:c.889A= NP_001166925.1:p.Ile297=
NM_001173455.1:c.796A= NP_001166926.1:p.Ile266=
NM_001173456.1:c.682A= NP_001166927.1:p.Ile228=
XM_011545531.1:c.910A= XP_011543833.1:p.Ile304=
XM_011545532.1:c.817A= XP_011543834.1:p.Ile273=
XM_017029574.2:c.796A= XP_016885063.1:p.Ile266=
NM_000284.4:c.775A= MANE Select NP_000275.1:p.Ile259=
NM_001173454.2:c.889A= NP_001166925.1:p.Ile297=
NM_001173455.2:c.796A= NP_001166926.1:p.Ile266=
NM_001173456.2:c.682A= NP_001166927.1:p.Ile228=