Canonical Allele Identifier: CA412394765
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355709C>A , CM000685.2:g.19355709C>A GRCh38
NC_000023.10:g.19373827C>A , CM000685.1:g.19373827C>A GRCh37
NC_000023.9:g.19283748C>A NCBI36
NG_016781.1:g.16817C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.804C>A ENSP00000348062.6:p.Cys268Ter
ENST00000379805.4:c.*475C>A ENSP00000369133.3:n.*475C>A
ENST00000417819.6:c.867C>A ENSP00000404616.2:p.Cys289Ter
ENST00000423505.6:c.897C>A ENSP00000406473.2:p.Cys299Ter
ENST00000481733.2:n.578C>A
ENST00000696704.1:c.*115C>A ENSP00000512823.1:n.*115C>A
ENST00000696705.1:c.*238C>A ENSP00000512824.1:n.*238C>A
ENST00000422285.7:c.783C>A MANE Select ENSP00000394382.2:p.Cys261Ter
ENST00000379804.1:c.-61C>A ENSP00000369132.1:n.-61C>A
ENST00000379806.9:c.897C>A ENSP00000369134.5:p.Cys299Ter
ENST00000422285.6:c.783C>A ENSP00000394382.2:p.Cys261Ter
ENST00000481733.1:n.211C>A
ENST00000540249.5:c.690C>A ENSP00000440761.1:p.Cys230Ter
ENST00000545074.5:c.804C>A ENSP00000438550.1:p.Cys268Ter
NM_000284.3:c.783C>A NP_000275.1:p.Cys261Ter
NM_001173454.1:c.897C>A NP_001166925.1:p.Cys299Ter
NM_001173455.1:c.804C>A NP_001166926.1:p.Cys268Ter
NM_001173456.1:c.690C>A NP_001166927.1:p.Cys230Ter
XM_011545531.1:c.918C>A XP_011543833.1:p.Cys306Ter
XM_011545532.1:c.825C>A XP_011543834.1:p.Cys275Ter
XM_017029574.2:c.804C>A XP_016885063.1:p.Cys268Ter
NM_000284.4:c.783C>A MANE Select NP_000275.1:p.Cys261Ter
NM_001173454.2:c.897C>A NP_001166925.1:p.Cys299Ter
NM_001173455.2:c.804C>A NP_001166926.1:p.Cys268Ter
NM_001173456.2:c.690C>A NP_001166927.1:p.Cys230Ter