Canonical Allele Identifier: CA2693251503
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359912del , CM000685.2:g.19359912del GRCh38
NC_000023.10:g.19378030del , CM000685.1:g.19378030del GRCh37
NC_000023.9:g.19287951del NCBI36
NG_016781.1:g.21020del
NG_021184.1:g.160350del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*259del ENSP00000348062.6:n.*259del
ENST00000423505.6:c.*259del ENSP00000406473.2:n.*259del
ENST00000696704.1:c.*764del ENSP00000512823.1:n.*764del
ENST00000696705.1:c.*887del ENSP00000512824.1:n.*887del
ENST00000422285.7:c.*259del MANE Select ENSP00000394382.2:n.*259del
ENST00000379806.9:c.*259del ENSP00000369134.5:n.*259del
ENST00000422285.6:c.*259del ENSP00000394382.2:n.*259del
ENST00000540249.5:c.*259del ENSP00000440761.1:n.*259del
ENST00000545074.5:c.*259del ENSP00000438550.1:n.*259del
NM_000284.3:c.*259del NP_000275.1:n.*259del
NM_001173454.1:c.*259del NP_001166925.1:n.*259del
NM_001173455.1:c.*259del NP_001166926.1:n.*259del
NM_001173456.1:c.*259del NP_001166927.1:n.*259del
XM_011545531.1:c.*259del XP_011543833.1:n.*259del
XM_011545532.1:c.*259del XP_011543834.1:n.*259del
NM_000284.4:c.*259del MANE Select NP_000275.1:n.*259del
NM_001173454.2:c.*259del NP_001166925.1:n.*259del
NM_001173455.2:c.*259del NP_001166926.1:n.*259del
NM_001173456.2:c.*259del NP_001166927.1:n.*259del