Canonical Allele Identifier: CA2418224609
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19357664A= , CM000685.2:g.19357664A= GRCh38
NC_000023.10:g.19375782A= , CM000685.1:g.19375782A= GRCh37
NC_000023.9:g.19285703A= NCBI36
NG_016781.1:g.18772A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.865A= ENSP00000348062.6:p.Met289=
ENST00000379805.4:c.*536A= ENSP00000369133.3:n.*536A=
ENST00000417819.6:c.928A= ENSP00000404616.2:p.Met310=
ENST00000423505.6:c.958A= ENSP00000406473.2:p.Met320=
ENST00000481733.2:n.639A=
ENST00000696704.1:c.*176A= ENSP00000512823.1:n.*176A=
ENST00000696705.1:c.*299A= ENSP00000512824.1:n.*299A=
ENST00000422285.7:c.844A= MANE Select ENSP00000394382.2:p.Met282=
ENST00000379804.1:c.1A= ENSP00000369132.1:p.Met1=
ENST00000379806.9:c.958A= ENSP00000369134.5:p.Met320=
ENST00000422285.6:c.844A= ENSP00000394382.2:p.Met282=
ENST00000478795.1:n.283A=
ENST00000481733.1:n.272A=
ENST00000540249.5:c.751A= ENSP00000440761.1:p.Met251=
ENST00000545074.5:c.865A= ENSP00000438550.1:p.Met289=
NM_000284.3:c.844A= NP_000275.1:p.Met282=
NM_001173454.1:c.958A= NP_001166925.1:p.Met320=
NM_001173455.1:c.865A= NP_001166926.1:p.Met289=
NM_001173456.1:c.751A= NP_001166927.1:p.Met251=
XM_011545531.1:c.979A= XP_011543833.1:p.Met327=
XM_011545532.1:c.886A= XP_011543834.1:p.Met296=
XM_017029574.2:c.865A= XP_016885063.1:p.Met289=
NM_000284.4:c.844A= MANE Select NP_000275.1:p.Met282=
NM_001173454.2:c.958A= NP_001166925.1:p.Met320=
NM_001173455.2:c.865A= NP_001166926.1:p.Met289=
NM_001173456.2:c.751A= NP_001166927.1:p.Met251=