Canonical Allele Identifier: CA412394751
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355702T>A , CM000685.2:g.19355702T>A GRCh38
NC_000023.10:g.19373820T>A , CM000685.1:g.19373820T>A GRCh37
NC_000023.9:g.19283741T>A NCBI36
NG_016781.1:g.16810T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.797T>A ENSP00000348062.6:p.Ile266Asn
ENST00000379805.4:c.*468T>A ENSP00000369133.3:n.*468T>A
ENST00000417819.6:c.860T>A ENSP00000404616.2:p.Ile287Asn
ENST00000423505.6:c.890T>A ENSP00000406473.2:p.Ile297Asn
ENST00000481733.2:n.571T>A
ENST00000696704.1:c.*108T>A ENSP00000512823.1:n.*108T>A
ENST00000696705.1:c.*231T>A ENSP00000512824.1:n.*231T>A
ENST00000422285.7:c.776T>A MANE Select ENSP00000394382.2:p.Ile259Asn
ENST00000379804.1:c.-68T>A ENSP00000369132.1:n.-68T>A
ENST00000379806.9:c.890T>A ENSP00000369134.5:p.Ile297Asn
ENST00000422285.6:c.776T>A ENSP00000394382.2:p.Ile259Asn
ENST00000481733.1:n.204T>A
ENST00000540249.5:c.683T>A ENSP00000440761.1:p.Ile228Asn
ENST00000545074.5:c.797T>A ENSP00000438550.1:p.Ile266Asn
NM_000284.3:c.776T>A NP_000275.1:p.Ile259Asn
NM_001173454.1:c.890T>A NP_001166925.1:p.Ile297Asn
NM_001173455.1:c.797T>A NP_001166926.1:p.Ile266Asn
NM_001173456.1:c.683T>A NP_001166927.1:p.Ile228Asn
XM_011545531.1:c.911T>A XP_011543833.1:p.Ile304Asn
XM_011545532.1:c.818T>A XP_011543834.1:p.Ile273Asn
XM_017029574.2:c.797T>A XP_016885063.1:p.Ile266Asn
NM_000284.4:c.776T>A MANE Select NP_000275.1:p.Ile259Asn
NM_001173454.2:c.890T>A NP_001166925.1:p.Ile297Asn
NM_001173455.2:c.797T>A NP_001166926.1:p.Ile266Asn
NM_001173456.2:c.683T>A NP_001166927.1:p.Ile228Asn