Canonical Allele Identifier: CA2418223673
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355543_19355545delinsGCC , CM000685.2:g.19355543_19355545delinsGCC GRCh38
NC_000023.10:g.19373661_19373663delinsGCC , CM000685.1:g.19373661_19373663delinsGCC GRCh37
NC_000023.9:g.19283582_19283584delinsGCC NCBI36
NG_016781.1:g.16651_16653delinsGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.780+39_780+41delinsGCC ENSP00000348062.6:n.780+39_780+41delinsGCC
ENST00000379805.4:c.*451+39_*451+41delinsGCC ENSP00000369133.3:n.*451+39_*451+41delinsGCC
ENST00000417819.6:c.843+39_843+41delinsGCC ENSP00000404616.2:n.843+39_843+41delinsGCC
ENST00000423505.6:c.873+39_873+41delinsGCC ENSP00000406473.2:n.873+39_873+41delinsGCC
ENST00000481733.2:n.554+39_554+41delinsGCC
ENST00000696704.1:c.*91+39_*91+41delinsGCC ENSP00000512823.1:n.*91+39_*91+41delinsGCC
ENST00000696705.1:c.*214+39_*214+41delinsGCC ENSP00000512824.1:n.*214+39_*214+41delinsGCC
ENST00000422285.7:c.759+39_759+41delinsGCC MANE Select ENSP00000394382.2:n.759+39_759+41delinsGCC
ENST00000379806.9:c.873+39_873+41delinsGCC ENSP00000369134.5:n.873+39_873+41delinsGCC
ENST00000422285.6:c.759+39_759+41delinsGCC ENSP00000394382.2:n.759+39_759+41delinsGCC
ENST00000481733.1:n.187+39_187+41delinsGCC
ENST00000540249.5:c.666+39_666+41delinsGCC ENSP00000440761.1:n.666+39_666+41delinsGCC
ENST00000545074.5:c.780+39_780+41delinsGCC ENSP00000438550.1:n.780+39_780+41delinsGCC
NM_000284.3:c.759+39_759+41delinsGCC NP_000275.1:n.759+39_759+41delinsGCC
NM_001173454.1:c.873+39_873+41delinsGCC NP_001166925.1:n.873+39_873+41delinsGCC
NM_001173455.1:c.780+39_780+41delinsGCC NP_001166926.1:n.780+39_780+41delinsGCC
NM_001173456.1:c.666+39_666+41delinsGCC NP_001166927.1:n.666+39_666+41delinsGCC
XM_011545531.1:c.894+39_894+41delinsGCC XP_011543833.1:n.894+39_894+41delinsGCC
XM_011545532.1:c.801+39_801+41delinsGCC XP_011543834.1:n.801+39_801+41delinsGCC
XM_017029574.2:c.780+39_780+41delinsGCC XP_016885063.1:n.780+39_780+41delinsGCC
NM_000284.4:c.759+39_759+41delinsGCC MANE Select NP_000275.1:n.759+39_759+41delinsGCC
NM_001173454.2:c.873+39_873+41delinsGCC NP_001166925.1:n.873+39_873+41delinsGCC
NM_001173455.2:c.780+39_780+41delinsGCC NP_001166926.1:n.780+39_780+41delinsGCC
NM_001173456.2:c.666+39_666+41delinsGCC NP_001166927.1:n.666+39_666+41delinsGCC