Canonical Allele Identifier: CA2693250501
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355551_19355553del , CM000685.2:g.19355551_19355553del GRCh38
NC_000023.10:g.19373669_19373671del , CM000685.1:g.19373669_19373671del GRCh37
NC_000023.9:g.19283590_19283592del NCBI36
NG_016781.1:g.16659_16661del

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.780+47_780+49del ENSP00000348062.6:n.780+47_780+49del
ENST00000379805.4:c.*451+47_*451+49del ENSP00000369133.3:n.*451+47_*451+49del
ENST00000417819.6:c.843+47_843+49del ENSP00000404616.2:n.843+47_843+49del
ENST00000423505.6:c.873+47_873+49del ENSP00000406473.2:n.873+47_873+49del
ENST00000481733.2:n.554+47_554+49del
ENST00000696704.1:c.*91+47_*91+49del ENSP00000512823.1:n.*91+47_*91+49del
ENST00000696705.1:c.*214+47_*214+49del ENSP00000512824.1:n.*214+47_*214+49del
ENST00000422285.7:c.759+47_759+49del MANE Select ENSP00000394382.2:n.759+47_759+49del
ENST00000379806.9:c.873+47_873+49del ENSP00000369134.5:n.873+47_873+49del
ENST00000422285.6:c.759+47_759+49del ENSP00000394382.2:n.759+47_759+49del
ENST00000481733.1:n.187+47_187+49del
ENST00000540249.5:c.666+47_666+49del ENSP00000440761.1:n.666+47_666+49del
ENST00000545074.5:c.780+47_780+49del ENSP00000438550.1:n.780+47_780+49del
NM_000284.3:c.759+47_759+49del NP_000275.1:n.759+47_759+49del
NM_001173454.1:c.873+47_873+49del NP_001166925.1:n.873+47_873+49del
NM_001173455.1:c.780+47_780+49del NP_001166926.1:n.780+47_780+49del
NM_001173456.1:c.666+47_666+49del NP_001166927.1:n.666+47_666+49del
XM_011545531.1:c.894+47_894+49del XP_011543833.1:n.894+47_894+49del
XM_011545532.1:c.801+47_801+49del XP_011543834.1:n.801+47_801+49del
XM_017029574.2:c.780+47_780+49del XP_016885063.1:n.780+47_780+49del
NM_000284.4:c.759+47_759+49del MANE Select NP_000275.1:n.759+47_759+49del
NM_001173454.2:c.873+47_873+49del NP_001166925.1:n.873+47_873+49del
NM_001173455.2:c.780+47_780+49del NP_001166926.1:n.780+47_780+49del
NM_001173456.2:c.666+47_666+49del NP_001166927.1:n.666+47_666+49del