Canonical Allele Identifier: CA412394668
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355488T>C , CM000685.2:g.19355488T>C GRCh38
NC_000023.10:g.19373606T>C , CM000685.1:g.19373606T>C GRCh37
NC_000023.9:g.19283527T>C NCBI36
NG_016781.1:g.16596T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.764T>C ENSP00000348062.6:p.Phe255Ser
ENST00000379805.4:c.*435T>C ENSP00000369133.3:n.*435T>C
ENST00000417819.6:c.827T>C ENSP00000404616.2:p.Phe276Ser
ENST00000423505.6:c.857T>C ENSP00000406473.2:p.Phe286Ser
ENST00000481733.2:n.538T>C
ENST00000696704.1:c.*75T>C ENSP00000512823.1:n.*75T>C
ENST00000696705.1:c.*198T>C ENSP00000512824.1:n.*198T>C
ENST00000422285.7:c.743T>C MANE Select ENSP00000394382.2:p.Phe248Ser
ENST00000379806.9:c.857T>C ENSP00000369134.5:p.Phe286Ser
ENST00000422285.6:c.743T>C ENSP00000394382.2:p.Phe248Ser
ENST00000481733.1:n.171T>C
ENST00000540249.5:c.650T>C ENSP00000440761.1:p.Phe217Ser
ENST00000545074.5:c.764T>C ENSP00000438550.1:p.Phe255Ser
NM_000284.3:c.743T>C NP_000275.1:p.Phe248Ser
NM_001173454.1:c.857T>C NP_001166925.1:p.Phe286Ser
NM_001173455.1:c.764T>C NP_001166926.1:p.Phe255Ser
NM_001173456.1:c.650T>C NP_001166927.1:p.Phe217Ser
XM_011545531.1:c.878T>C XP_011543833.1:p.Phe293Ser
XM_011545532.1:c.785T>C XP_011543834.1:p.Phe262Ser
XM_017029574.2:c.764T>C XP_016885063.1:p.Phe255Ser
NM_000284.4:c.743T>C MANE Select NP_000275.1:p.Phe248Ser
NM_001173454.2:c.857T>C NP_001166925.1:p.Phe286Ser
NM_001173455.2:c.764T>C NP_001166926.1:p.Phe255Ser
NM_001173456.2:c.650T>C NP_001166927.1:p.Phe217Ser