Canonical Allele Identifier: CA327029400
Gene: PDHA1 HGNC NCBI

Linked Data

dbSNP Id: rs1023820890
gnomAD v3: X-19357574-G-A
gnomAD v4: X-19357574-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19357574G>A , CM000685.2:g.19357574G>A GRCh38
NC_000023.10:g.19375692G>A , CM000685.1:g.19375692G>A GRCh37
NC_000023.9:g.19285613G>A NCBI36
NG_016781.1:g.18682G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.853-78G>A ENSP00000348062.6:n.853-78G>A
ENST00000379805.4:c.*524-78G>A ENSP00000369133.3:n.*524-78G>A
ENST00000417819.6:c.916-78G>A ENSP00000404616.2:n.916-78G>A
ENST00000423505.6:c.946-78G>A ENSP00000406473.2:n.946-78G>A
ENST00000481733.2:n.627-78G>A
ENST00000696704.1:c.*164-78G>A ENSP00000512823.1:n.*164-78G>A
ENST00000696705.1:c.*287-78G>A ENSP00000512824.1:n.*287-78G>A
ENST00000422285.7:c.832-78G>A MANE Select ENSP00000394382.2:n.832-78G>A
ENST00000379804.1:c.-12-78G>A ENSP00000369132.1:n.-12-78G>A
ENST00000379806.9:c.946-78G>A ENSP00000369134.5:n.946-78G>A
ENST00000422285.6:c.832-78G>A ENSP00000394382.2:n.832-78G>A
ENST00000478795.1:n.193G>A
ENST00000481733.1:n.260-78G>A
ENST00000540249.5:c.739-78G>A ENSP00000440761.1:n.739-78G>A
ENST00000545074.5:c.853-78G>A ENSP00000438550.1:n.853-78G>A
NM_000284.3:c.832-78G>A NP_000275.1:n.832-78G>A
NM_001173454.1:c.946-78G>A NP_001166925.1:n.946-78G>A
NM_001173455.1:c.853-78G>A NP_001166926.1:n.853-78G>A
NM_001173456.1:c.739-78G>A NP_001166927.1:n.739-78G>A
XM_011545531.1:c.967-78G>A XP_011543833.1:n.967-78G>A
XM_011545532.1:c.874-78G>A XP_011543834.1:n.874-78G>A
XM_017029574.2:c.853-78G>A XP_016885063.1:n.853-78G>A
NM_000284.4:c.832-78G>A MANE Select NP_000275.1:n.832-78G>A
NM_001173454.2:c.946-78G>A NP_001166925.1:n.946-78G>A
NM_001173455.2:c.853-78G>A NP_001166926.1:n.853-78G>A
NM_001173456.2:c.739-78G>A NP_001166927.1:n.739-78G>A