Canonical Allele Identifier: CA2418222716
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19352858A= , CM000685.2:g.19352858A= GRCh38
NC_000023.10:g.19370976A= , CM000685.1:g.19370976A= GRCh37
NC_000023.9:g.19280897A= NCBI36
NG_016781.1:g.13966A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.440-224A= ENSP00000348062.6:n.440-224A=
ENST00000379805.4:c.419-224A= ENSP00000369133.3:n.419-224A=
ENST00000417819.6:c.503-224A= ENSP00000404616.2:n.503-224A=
ENST00000423505.6:c.533-224A= ENSP00000406473.2:n.533-224A=
ENST00000696704.1:c.418+1451A= ENSP00000512823.1:n.418+1451A=
ENST00000696705.1:c.418+1451A= ENSP00000512824.1:n.418+1451A=
ENST00000422285.7:c.419-224A= MANE Select ENSP00000394382.2:n.419-224A=
ENST00000355808.9:c.440-224A= ENSP00000348062.5:n.440-224A=
ENST00000379805.3:c.419-224A= ENSP00000369133.3:n.419-224A=
ENST00000379806.9:c.533-224A= ENSP00000369134.5:n.533-224A=
ENST00000422285.6:c.419-224A= ENSP00000394382.2:n.419-224A=
ENST00000423505.5:c.533-224A= ENSP00000406473.1:n.533-224A=
ENST00000479146.1:n.30A=
ENST00000540249.5:c.419-224A= ENSP00000440761.1:n.419-224A=
ENST00000545074.5:c.440-224A= ENSP00000438550.1:n.440-224A=
NM_000284.3:c.419-224A= NP_000275.1:n.419-224A=
NM_001173454.1:c.533-224A= NP_001166925.1:n.533-224A=
NM_001173455.1:c.440-224A= NP_001166926.1:n.440-224A=
NM_001173456.1:c.419-224A= NP_001166927.1:n.419-224A=
XM_011545531.1:c.554-224A= XP_011543833.1:n.554-224A=
XM_011545532.1:c.554-224A= XP_011543834.1:n.554-224A=
XM_017029574.2:c.533-224A= XP_016885063.1:n.533-224A=
NM_000284.4:c.419-224A= MANE Select NP_000275.1:n.419-224A=
NM_001173454.2:c.533-224A= NP_001166925.1:n.533-224A=
NM_001173455.2:c.440-224A= NP_001166926.1:n.440-224A=
NM_001173456.2:c.419-224A= NP_001166927.1:n.419-224A=