Canonical Allele Identifier: CA412394477
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355406A>T , CM000685.2:g.19355406A>T GRCh38
NC_000023.10:g.19373524A>T , CM000685.1:g.19373524A>T GRCh37
NC_000023.9:g.19283445A>T NCBI36
NG_016781.1:g.16514A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.682A>T ENSP00000348062.6:p.Ile228Phe
ENST00000379805.4:c.*353A>T ENSP00000369133.3:n.*353A>T
ENST00000417819.6:c.745A>T ENSP00000404616.2:p.Ile249Phe
ENST00000423505.6:c.775A>T ENSP00000406473.2:p.Ile259Phe
ENST00000481733.2:n.456A>T
ENST00000696704.1:c.476A>T ENSP00000512823.1:p.His159Leu
ENST00000696705.1:c.*116A>T ENSP00000512824.1:n.*116A>T
ENST00000422285.7:c.661A>T MANE Select ENSP00000394382.2:p.Ile221Phe
ENST00000379806.9:c.775A>T ENSP00000369134.5:p.Ile259Phe
ENST00000422285.6:c.661A>T ENSP00000394382.2:p.Ile221Phe
ENST00000479146.1:n.496A>T
ENST00000481733.1:n.89A>T
ENST00000540249.5:c.568A>T ENSP00000440761.1:p.Ile190Phe
ENST00000545074.5:c.682A>T ENSP00000438550.1:p.Ile228Phe
NM_000284.3:c.661A>T NP_000275.1:p.Ile221Phe
NM_001173454.1:c.775A>T NP_001166925.1:p.Ile259Phe
NM_001173455.1:c.682A>T NP_001166926.1:p.Ile228Phe
NM_001173456.1:c.568A>T NP_001166927.1:p.Ile190Phe
XM_011545531.1:c.796A>T XP_011543833.1:p.Ile266Phe
XM_011545532.1:c.703A>T XP_011543834.1:p.Ile235Phe
XM_017029574.2:c.682A>T XP_016885063.1:p.Ile228Phe
NM_000284.4:c.661A>T MANE Select NP_000275.1:p.Ile221Phe
NM_001173454.2:c.775A>T NP_001166925.1:p.Ile259Phe
NM_001173455.2:c.682A>T NP_001166926.1:p.Ile228Phe
NM_001173456.2:c.568A>T NP_001166927.1:p.Ile190Phe