Canonical Allele Identifier: CA412394610
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355464C>G , CM000685.2:g.19355464C>G GRCh38
NC_000023.10:g.19373582C>G , CM000685.1:g.19373582C>G GRCh37
NC_000023.9:g.19283503C>G NCBI36
NG_016781.1:g.16572C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.740C>G ENSP00000348062.6:p.Thr247Ser
ENST00000379805.4:c.*411C>G ENSP00000369133.3:n.*411C>G
ENST00000417819.6:c.803C>G ENSP00000404616.2:p.Thr268Ser
ENST00000423505.6:c.833C>G ENSP00000406473.2:p.Thr278Ser
ENST00000481733.2:n.514C>G
ENST00000696704.1:c.*51C>G ENSP00000512823.1:n.*51C>G
ENST00000696705.1:c.*174C>G ENSP00000512824.1:n.*174C>G
ENST00000422285.7:c.719C>G MANE Select ENSP00000394382.2:p.Thr240Ser
ENST00000379806.9:c.833C>G ENSP00000369134.5:p.Thr278Ser
ENST00000422285.6:c.719C>G ENSP00000394382.2:p.Thr240Ser
ENST00000481733.1:n.147C>G
ENST00000540249.5:c.626C>G ENSP00000440761.1:p.Thr209Ser
ENST00000545074.5:c.740C>G ENSP00000438550.1:p.Thr247Ser
NM_000284.3:c.719C>G NP_000275.1:p.Thr240Ser
NM_001173454.1:c.833C>G NP_001166925.1:p.Thr278Ser
NM_001173455.1:c.740C>G NP_001166926.1:p.Thr247Ser
NM_001173456.1:c.626C>G NP_001166927.1:p.Thr209Ser
XM_011545531.1:c.854C>G XP_011543833.1:p.Thr285Ser
XM_011545532.1:c.761C>G XP_011543834.1:p.Thr254Ser
XM_017029574.2:c.740C>G XP_016885063.1:p.Thr247Ser
NM_000284.4:c.719C>G MANE Select NP_000275.1:p.Thr240Ser
NM_001173454.2:c.833C>G NP_001166925.1:p.Thr278Ser
NM_001173455.2:c.740C>G NP_001166926.1:p.Thr247Ser
NM_001173456.2:c.626C>G NP_001166927.1:p.Thr209Ser