Canonical Allele Identifier: CA10362983
Community Standard Title: NM_000284.4(PDHA1):c.98A>T (p.Asp33Val)
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19349352A>T , CM000685.2:g.19349352A>T GRCh38
NC_000023.10:g.19367470A>T , CM000685.1:g.19367470A>T GRCh37
NC_000023.9:g.19277391A>T NCBI36
NG_016781.1:g.10460A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000284.4:c.98A>T MANE Select NP_000275.1:p.Asp33Val
ENST00000422285.7:c.98A>T MANE Select ENSP00000394382.2:p.Asp33Val
NM_000284.3:c.98A>T NP_000275.1:p.Asp33Val
NM_001173454.1:c.212A>T NP_001166925.1:p.Asp71Val
NM_001173454.2:c.212A>T NP_001166925.1:p.Asp71Val
NM_001173455.1:c.98A>T NP_001166926.1:p.Asp33Val
NM_001173455.2:c.98A>T NP_001166926.1:p.Asp33Val
NM_001173456.1:c.98A>T NP_001166927.1:p.Asp33Val
NM_001173456.2:c.98A>T NP_001166927.1:p.Asp33Val
ENST00000355808.10:c.98A>T ENSP00000348062.6:p.Asp33Val
ENST00000355808.9:c.98A>T ENSP00000348062.5:p.Asp33Val
ENST00000379805.3:c.98A>T ENSP00000369133.3:p.Asp33Val
ENST00000379805.4:c.98A>T ENSP00000369133.3:p.Asp33Val
ENST00000379806.9:c.212A>T ENSP00000369134.5:p.Asp71Val
ENST00000417819.5:c.182A>T ENSP00000404616.1:p.Asp61Val
ENST00000417819.6:c.182A>T ENSP00000404616.2:p.Asp61Val
ENST00000422285.6:c.98A>T ENSP00000394382.2:p.Asp33Val
ENST00000423505.5:c.212A>T ENSP00000406473.1:p.Asp71Val
ENST00000423505.6:c.212A>T ENSP00000406473.2:p.Asp71Val
ENST00000492364.1:n.200A>T
ENST00000540249.5:c.98A>T ENSP00000440761.1:p.Asp33Val
ENST00000545074.5:c.98A>T ENSP00000438550.1:p.Asp33Val
ENST00000696704.1:c.98A>T ENSP00000512823.1:p.Asp33Val
ENST00000696705.1:c.98A>T ENSP00000512824.1:p.Asp33Val
XM_011545531.1:c.212A>T XP_011543833.1:p.Asp71Val
XM_011545532.1:c.212A>T XP_011543834.1:p.Asp71Val
XM_017029574.2:c.212A>T XP_016885063.1:p.Asp71Val