Canonical Allele Identifier: CA412389647
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19349946C>G , CM000685.2:g.19349946C>G GRCh38
NC_000023.10:g.19368064C>G , CM000685.1:g.19368064C>G GRCh37
NC_000023.9:g.19277985C>G NCBI36
NG_016781.1:g.11054C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.127C>G ENSP00000348062.6:p.Leu43Val
ENST00000379805.4:c.127C>G ENSP00000369133.3:p.Leu43Val
ENST00000417819.6:c.211C>G ENSP00000404616.2:p.Leu71Val
ENST00000423505.6:c.241C>G ENSP00000406473.2:p.Leu81Val
ENST00000696704.1:c.127C>G ENSP00000512823.1:p.Leu43Val
ENST00000696705.1:c.127C>G ENSP00000512824.1:p.Leu43Val
ENST00000422285.7:c.127C>G MANE Select ENSP00000394382.2:p.Leu43Val
ENST00000355808.9:c.127C>G ENSP00000348062.5:p.Leu43Val
ENST00000379805.3:c.127C>G ENSP00000369133.3:p.Leu43Val
ENST00000379806.9:c.241C>G ENSP00000369134.5:p.Leu81Val
ENST00000417819.5:c.211C>G ENSP00000404616.1:p.Leu71Val
ENST00000422285.6:c.127C>G ENSP00000394382.2:p.Leu43Val
ENST00000423505.5:c.241C>G ENSP00000406473.1:p.Leu81Val
ENST00000492364.1:n.229C>G
ENST00000540249.5:c.127C>G ENSP00000440761.1:p.Leu43Val
ENST00000545074.5:c.127C>G ENSP00000438550.1:p.Leu43Val
NM_000284.3:c.127C>G NP_000275.1:p.Leu43Val
NM_001173454.1:c.241C>G NP_001166925.1:p.Leu81Val
NM_001173455.1:c.127C>G NP_001166926.1:p.Leu43Val
NM_001173456.1:c.127C>G NP_001166927.1:p.Leu43Val
XM_011545531.1:c.241C>G XP_011543833.1:p.Leu81Val
XM_011545532.1:c.241C>G XP_011543834.1:p.Leu81Val
XM_017029574.2:c.241C>G XP_016885063.1:p.Leu81Val
NM_000284.4:c.127C>G MANE Select NP_000275.1:p.Leu43Val
NM_001173454.2:c.241C>G NP_001166925.1:p.Leu81Val
NM_001173455.2:c.127C>G NP_001166926.1:p.Leu43Val
NM_001173456.2:c.127C>G NP_001166927.1:p.Leu43Val