Canonical Allele Identifier: CA2418225668
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359703C= , CM000685.2:g.19359703C= GRCh38
NC_000023.10:g.19377821C= , CM000685.1:g.19377821C= GRCh37
NC_000023.9:g.19287742C= NCBI36
NG_016781.1:g.20811C=
NG_021184.1:g.160559G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*50C= ENSP00000348062.6:n.*50C=
ENST00000379805.4:c.*915C= ENSP00000369133.3:n.*915C=
ENST00000417819.6:c.*50C= ENSP00000404616.2:n.*50C=
ENST00000423505.6:c.*50C= ENSP00000406473.2:n.*50C=
ENST00000481733.2:n.1018C=
ENST00000696704.1:c.*555C= ENSP00000512823.1:n.*555C=
ENST00000696705.1:c.*678C= ENSP00000512824.1:n.*678C=
ENST00000422285.7:c.*50C= MANE Select ENSP00000394382.2:n.*50C=
ENST00000379804.1:c.*50C= ENSP00000369132.1:n.*50C=
ENST00000379806.9:c.*50C= ENSP00000369134.5:n.*50C=
ENST00000422285.6:c.*50C= ENSP00000394382.2:n.*50C=
ENST00000478795.1:n.662C=
ENST00000540249.5:c.*50C= ENSP00000440761.1:n.*50C=
ENST00000545074.5:c.*50C= ENSP00000438550.1:n.*50C=
NM_000284.3:c.*50C= NP_000275.1:n.*50C=
NM_001173454.1:c.*50C= NP_001166925.1:n.*50C=
NM_001173455.1:c.*50C= NP_001166926.1:n.*50C=
NM_001173456.1:c.*50C= NP_001166927.1:n.*50C=
XM_011545531.1:c.*50C= XP_011543833.1:n.*50C=
XM_011545532.1:c.*50C= XP_011543834.1:n.*50C=
XM_017029574.2:c.*50C= XP_016885063.1:n.*50C=
NM_000284.4:c.*50C= MANE Select NP_000275.1:n.*50C=
NM_001173454.2:c.*50C= NP_001166925.1:n.*50C=
NM_001173455.2:c.*50C= NP_001166926.1:n.*50C=
NM_001173456.2:c.*50C= NP_001166927.1:n.*50C=