Canonical Allele Identifier: CA1131434610
Gene: PDHA1 HGNC NCBI

Linked Data

dbSNP Id: rs2063248950
gnomAD v3: X-19359654-G-C
gnomAD v4: X-19359654-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359654G>C , CM000685.2:g.19359654G>C GRCh38
NC_000023.10:g.19377772G>C , CM000685.1:g.19377772G>C GRCh37
NC_000023.9:g.19287693G>C NCBI36
NG_016781.1:g.20762G>C
NG_021184.1:g.160608C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*1G>C ENSP00000348062.6:n.*1G>C
ENST00000379805.4:c.*866G>C ENSP00000369133.3:n.*866G>C
ENST00000417819.6:c.*1G>C ENSP00000404616.2:n.*1G>C
ENST00000423505.6:c.*1G>C ENSP00000406473.2:n.*1G>C
ENST00000481733.2:n.969G>C
ENST00000696704.1:c.*506G>C ENSP00000512823.1:n.*506G>C
ENST00000696705.1:c.*629G>C ENSP00000512824.1:n.*629G>C
ENST00000422285.7:c.*1G>C MANE Select ENSP00000394382.2:n.*1G>C
ENST00000379804.1:c.*1G>C ENSP00000369132.1:n.*1G>C
ENST00000379806.9:c.*1G>C ENSP00000369134.5:n.*1G>C
ENST00000422285.6:c.*1G>C ENSP00000394382.2:n.*1G>C
ENST00000478795.1:n.613G>C
ENST00000540249.5:c.*1G>C ENSP00000440761.1:n.*1G>C
ENST00000545074.5:c.*1G>C ENSP00000438550.1:n.*1G>C
NM_000284.3:c.*1G>C NP_000275.1:n.*1G>C
NM_001173454.1:c.*1G>C NP_001166925.1:n.*1G>C
NM_001173455.1:c.*1G>C NP_001166926.1:n.*1G>C
NM_001173456.1:c.*1G>C NP_001166927.1:n.*1G>C
XM_011545531.1:c.*1G>C XP_011543833.1:n.*1G>C
XM_011545532.1:c.*1G>C XP_011543834.1:n.*1G>C
XM_017029574.2:c.*1G>C XP_016885063.1:n.*1G>C
NM_000284.4:c.*1G>C MANE Select NP_000275.1:n.*1G>C
NM_001173454.2:c.*1G>C NP_001166925.1:n.*1G>C
NM_001173455.2:c.*1G>C NP_001166926.1:n.*1G>C
NM_001173456.2:c.*1G>C NP_001166927.1:n.*1G>C