Canonical Allele Identifier: CA412394606
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355463A>T , CM000685.2:g.19355463A>T GRCh38
NC_000023.10:g.19373581A>T , CM000685.1:g.19373581A>T GRCh37
NC_000023.9:g.19283502A>T NCBI36
NG_016781.1:g.16571A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.739A>T ENSP00000348062.6:p.Thr247Ser
ENST00000379805.4:c.*410A>T ENSP00000369133.3:n.*410A>T
ENST00000417819.6:c.802A>T ENSP00000404616.2:p.Thr268Ser
ENST00000423505.6:c.832A>T ENSP00000406473.2:p.Thr278Ser
ENST00000481733.2:n.513A>T
ENST00000696704.1:c.*50A>T ENSP00000512823.1:n.*50A>T
ENST00000696705.1:c.*173A>T ENSP00000512824.1:n.*173A>T
ENST00000422285.7:c.718A>T MANE Select ENSP00000394382.2:p.Thr240Ser
ENST00000379806.9:c.832A>T ENSP00000369134.5:p.Thr278Ser
ENST00000422285.6:c.718A>T ENSP00000394382.2:p.Thr240Ser
ENST00000481733.1:n.146A>T
ENST00000540249.5:c.625A>T ENSP00000440761.1:p.Thr209Ser
ENST00000545074.5:c.739A>T ENSP00000438550.1:p.Thr247Ser
NM_000284.3:c.718A>T NP_000275.1:p.Thr240Ser
NM_001173454.1:c.832A>T NP_001166925.1:p.Thr278Ser
NM_001173455.1:c.739A>T NP_001166926.1:p.Thr247Ser
NM_001173456.1:c.625A>T NP_001166927.1:p.Thr209Ser
XM_011545531.1:c.853A>T XP_011543833.1:p.Thr285Ser
XM_011545532.1:c.760A>T XP_011543834.1:p.Thr254Ser
XM_017029574.2:c.739A>T XP_016885063.1:p.Thr247Ser
NM_000284.4:c.718A>T MANE Select NP_000275.1:p.Thr240Ser
NM_001173454.2:c.832A>T NP_001166925.1:p.Thr278Ser
NM_001173455.2:c.739A>T NP_001166926.1:p.Thr247Ser
NM_001173456.2:c.625A>T NP_001166927.1:p.Thr209Ser