Canonical Allele Identifier: CA2418222095
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19351289C= , CM000685.2:g.19351289C= GRCh38
NC_000023.10:g.19369407C= , CM000685.1:g.19369407C= GRCh37
NC_000023.9:g.19279328C= NCBI36
NG_016781.1:g.12397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.321C= ENSP00000348062.6:p.Cys107=
ENST00000379805.4:c.300C= ENSP00000369133.3:p.Cys100=
ENST00000417819.6:c.384C= ENSP00000404616.2:p.Cys128=
ENST00000423505.6:c.414C= ENSP00000406473.2:p.Cys138=
ENST00000696704.1:c.300C= ENSP00000512823.1:p.Cys100=
ENST00000696705.1:c.300C= ENSP00000512824.1:p.Cys100=
ENST00000422285.7:c.300C= MANE Select ENSP00000394382.2:p.Cys100=
ENST00000355808.9:c.321C= ENSP00000348062.5:p.Cys107=
ENST00000379805.3:c.300C= ENSP00000369133.3:p.Cys100=
ENST00000379806.9:c.414C= ENSP00000369134.5:p.Cys138=
ENST00000422285.6:c.300C= ENSP00000394382.2:p.Cys100=
ENST00000423505.5:c.414C= ENSP00000406473.1:p.Cys138=
ENST00000492364.1:n.402C=
ENST00000540249.5:c.300C= ENSP00000440761.1:p.Cys100=
ENST00000545074.5:c.321C= ENSP00000438550.1:p.Cys107=
NM_000284.3:c.300C= NP_000275.1:p.Cys100=
NM_001173454.1:c.414C= NP_001166925.1:p.Cys138=
NM_001173455.1:c.321C= NP_001166926.1:p.Cys107=
NM_001173456.1:c.300C= NP_001166927.1:p.Cys100=
XM_011545531.1:c.435C= XP_011543833.1:p.Cys145=
XM_011545532.1:c.435C= XP_011543834.1:p.Cys145=
XM_017029574.2:c.414C= XP_016885063.1:p.Cys138=
NM_000284.4:c.300C= MANE Select NP_000275.1:p.Cys100=
NM_001173454.2:c.414C= NP_001166925.1:p.Cys138=
NM_001173455.2:c.321C= NP_001166926.1:p.Cys107=
NM_001173456.2:c.300C= NP_001166927.1:p.Cys100=