Canonical Allele Identifier: CA2693251427
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359789_19359801del , CM000685.2:g.19359789_19359801del GRCh38
NC_000023.10:g.19377907_19377919del , CM000685.1:g.19377907_19377919del GRCh37
NC_000023.9:g.19287828_19287840del NCBI36
NG_016781.1:g.20897_20909del
NG_021184.1:g.160464_160476del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*136_*148del ENSP00000348062.6:n.*136_*148del
ENST00000379805.4:c.*1001_*1013del ENSP00000369133.3:n.*1001_*1013del
ENST00000417819.6:c.*136_*148del ENSP00000404616.2:n.*136_*148del
ENST00000423505.6:c.*136_*148del ENSP00000406473.2:n.*136_*148del
ENST00000481733.2:n.1104_1116del
ENST00000696704.1:c.*641_*653del ENSP00000512823.1:n.*641_*653del
ENST00000696705.1:c.*764_*776del ENSP00000512824.1:n.*764_*776del
ENST00000422285.7:c.*136_*148del MANE Select ENSP00000394382.2:n.*136_*148del
ENST00000379804.1:c.*136_*148del ENSP00000369132.1:n.*136_*148del
ENST00000379806.9:c.*136_*148del ENSP00000369134.5:n.*136_*148del
ENST00000422285.6:c.*136_*148del ENSP00000394382.2:n.*136_*148del
ENST00000478795.1:n.748_760del
ENST00000540249.5:c.*136_*148del ENSP00000440761.1:n.*136_*148del
ENST00000545074.5:c.*136_*148del ENSP00000438550.1:n.*136_*148del
NM_000284.3:c.*136_*148del NP_000275.1:n.*136_*148del
NM_001173454.1:c.*136_*148del NP_001166925.1:n.*136_*148del
NM_001173455.1:c.*136_*148del NP_001166926.1:n.*136_*148del
NM_001173456.1:c.*136_*148del NP_001166927.1:n.*136_*148del
XM_011545531.1:c.*136_*148del XP_011543833.1:n.*136_*148del
XM_011545532.1:c.*136_*148del XP_011543834.1:n.*136_*148del
XM_017029574.2:c.*136_*148del XP_016885063.1:n.*136_*148del
NM_000284.4:c.*136_*148del MANE Select NP_000275.1:n.*136_*148del
NM_001173454.2:c.*136_*148del NP_001166925.1:n.*136_*148del
NM_001173455.2:c.*136_*148del NP_001166926.1:n.*136_*148del
NM_001173456.2:c.*136_*148del NP_001166927.1:n.*136_*148del