Canonical Allele Identifier: CA2418225625
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359644A= , CM000685.2:g.19359644A= GRCh38
NC_000023.10:g.19377762A= , CM000685.1:g.19377762A= GRCh37
NC_000023.9:g.19287683A= NCBI36
NG_016781.1:g.20752A=
NG_021184.1:g.160618T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.1185A= ENSP00000348062.6:p.Ser395=
ENST00000379805.4:c.*856A= ENSP00000369133.3:n.*856A=
ENST00000417819.6:c.1248A= ENSP00000404616.2:p.Ser416=
ENST00000423505.6:c.1278A= ENSP00000406473.2:p.Ser426=
ENST00000481733.2:n.959A=
ENST00000696704.1:c.*496A= ENSP00000512823.1:n.*496A=
ENST00000696705.1:c.*619A= ENSP00000512824.1:n.*619A=
ENST00000422285.7:c.1164A= MANE Select ENSP00000394382.2:p.Ser388=
ENST00000379804.1:c.321A= ENSP00000369132.1:p.Ser107=
ENST00000379806.9:c.1278A= ENSP00000369134.5:p.Ser426=
ENST00000422285.6:c.1164A= ENSP00000394382.2:p.Ser388=
ENST00000478795.1:n.603A=
ENST00000540249.5:c.1071A= ENSP00000440761.1:p.Ser357=
ENST00000545074.5:c.1185A= ENSP00000438550.1:p.Ser395=
NM_000284.3:c.1164A= NP_000275.1:p.Ser388=
NM_001173454.1:c.1278A= NP_001166925.1:p.Ser426=
NM_001173455.1:c.1185A= NP_001166926.1:p.Ser395=
NM_001173456.1:c.1071A= NP_001166927.1:p.Ser357=
XM_011545531.1:c.1299A= XP_011543833.1:p.Ser433=
XM_011545532.1:c.1206A= XP_011543834.1:p.Ser402=
XM_017029574.2:c.1185A= XP_016885063.1:p.Ser395=
NM_000284.4:c.1164A= MANE Select NP_000275.1:p.Ser388=
NM_001173454.2:c.1278A= NP_001166925.1:p.Ser426=
NM_001173455.2:c.1185A= NP_001166926.1:p.Ser395=
NM_001173456.2:c.1071A= NP_001166927.1:p.Ser357=