Canonical Allele Identifier: CA873740888
Gene: PDHA1 HGNC NCBI

Linked Data

dbSNP Id: rs1313330293

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19357867del , CM000685.2:g.19357867del GRCh38
NC_000023.10:g.19375985del , CM000685.1:g.19375985del GRCh37
NC_000023.9:g.19285906del NCBI36
NG_016781.1:g.18975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.920+148del ENSP00000348062.6:n.920+148del
ENST00000379805.4:c.*591+148del ENSP00000369133.3:n.*591+148del
ENST00000417819.6:c.983+148del ENSP00000404616.2:n.983+148del
ENST00000423505.6:c.1013+148del ENSP00000406473.2:n.1013+148del
ENST00000481733.2:n.694+148del
ENST00000696704.1:c.*231+148del ENSP00000512823.1:n.*231+148del
ENST00000696705.1:c.*354+148del ENSP00000512824.1:n.*354+148del
ENST00000422285.7:c.899+148del MANE Select ENSP00000394382.2:n.899+148del
ENST00000379804.1:c.56+148del ENSP00000369132.1:n.56+148del
ENST00000379806.9:c.1013+148del ENSP00000369134.5:n.1013+148del
ENST00000422285.6:c.899+148del ENSP00000394382.2:n.899+148del
ENST00000478795.1:n.338+148del
ENST00000481733.1:n.327+148del
ENST00000540249.5:c.806+148del ENSP00000440761.1:n.806+148del
ENST00000545074.5:c.920+148del ENSP00000438550.1:n.920+148del
NM_000284.3:c.899+148del NP_000275.1:n.899+148del
NM_001173454.1:c.1013+148del NP_001166925.1:n.1013+148del
NM_001173455.1:c.920+148del NP_001166926.1:n.920+148del
NM_001173456.1:c.806+148del NP_001166927.1:n.806+148del
XM_011545531.1:c.1034+148del XP_011543833.1:n.1034+148del
XM_011545532.1:c.941+148del XP_011543834.1:n.941+148del
XM_017029574.2:c.920+148del XP_016885063.1:n.920+148del
NM_000284.4:c.899+148del MANE Select NP_000275.1:n.899+148del
NM_001173454.2:c.1013+148del NP_001166925.1:n.1013+148del
NM_001173455.2:c.920+148del NP_001166926.1:n.920+148del
NM_001173456.2:c.806+148del NP_001166927.1:n.806+148del