Canonical Allele Identifier: CA2418223572
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355308G= , CM000685.2:g.19355308G= GRCh38
NC_000023.10:g.19373426G= , CM000685.1:g.19373426G= GRCh37
NC_000023.9:g.19283347G= NCBI36
NG_016781.1:g.16416G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.625-41G= ENSP00000348062.6:n.625-41G=
ENST00000379805.4:c.*296-41G= ENSP00000369133.3:n.*296-41G=
ENST00000417819.6:c.688-41G= ENSP00000404616.2:n.688-41G=
ENST00000423505.6:c.718-41G= ENSP00000406473.2:n.718-41G=
ENST00000481733.2:n.358G=
ENST00000696704.1:c.419-41G= ENSP00000512823.1:n.419-41G=
ENST00000696705.1:c.*59-41G= ENSP00000512824.1:n.*59-41G=
ENST00000422285.7:c.604-41G= MANE Select ENSP00000394382.2:n.604-41G=
ENST00000379806.9:c.718-41G= ENSP00000369134.5:n.718-41G=
ENST00000422285.6:c.604-41G= ENSP00000394382.2:n.604-41G=
ENST00000479146.1:n.439-41G=
ENST00000540249.5:c.511-41G= ENSP00000440761.1:n.511-41G=
ENST00000545074.5:c.625-41G= ENSP00000438550.1:n.625-41G=
NM_000284.3:c.604-41G= NP_000275.1:n.604-41G=
NM_001173454.1:c.718-41G= NP_001166925.1:n.718-41G=
NM_001173455.1:c.625-41G= NP_001166926.1:n.625-41G=
NM_001173456.1:c.511-41G= NP_001166927.1:n.511-41G=
XM_011545531.1:c.739-41G= XP_011543833.1:n.739-41G=
XM_011545532.1:c.646-41G= XP_011543834.1:n.646-41G=
XM_017029574.2:c.625-41G= XP_016885063.1:n.625-41G=
NM_000284.4:c.604-41G= MANE Select NP_000275.1:n.604-41G=
NM_001173454.2:c.718-41G= NP_001166925.1:n.718-41G=
NM_001173455.2:c.625-41G= NP_001166926.1:n.625-41G=
NM_001173456.2:c.511-41G= NP_001166927.1:n.511-41G=