Canonical Allele Identifier: CA515485857
Gene: PDHA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.19371207A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19353089A>G , CM000685.2:g.19353089A>G GRCh38
NC_000023.10:g.19371207A>G , CM000685.1:g.19371207A>G GRCh37
NC_000023.9:g.19281128A>G NCBI36
NG_016781.1:g.14197A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.447A>G ENSP00000348062.6:p.Lys149=
ENST00000379805.4:c.426A>G ENSP00000369133.3:p.Lys142=
ENST00000417819.6:c.510A>G ENSP00000404616.2:p.Lys170=
ENST00000423505.6:c.540A>G ENSP00000406473.2:p.Lys180=
ENST00000696704.1:c.418+1682A>G ENSP00000512823.1:n.418+1682A>G
ENST00000696705.1:c.419-1402A>G ENSP00000512824.1:n.419-1402A>G
ENST00000422285.7:c.426A>G MANE Select ENSP00000394382.2:p.Lys142=
ENST00000355808.9:c.447A>G ENSP00000348062.5:p.Lys149=
ENST00000379805.3:c.426A>G ENSP00000369133.3:p.Lys142=
ENST00000379806.9:c.540A>G ENSP00000369134.5:p.Lys180=
ENST00000422285.6:c.426A>G ENSP00000394382.2:p.Lys142=
ENST00000423505.5:c.540A>G ENSP00000406473.1:p.Lys180=
ENST00000479146.1:n.261A>G
ENST00000540249.5:c.426A>G ENSP00000440761.1:p.Lys142=
ENST00000545074.5:c.447A>G ENSP00000438550.1:p.Lys149=
NM_000284.3:c.426A>G NP_000275.1:p.Lys142=
NM_001173454.1:c.540A>G NP_001166925.1:p.Lys180=
NM_001173455.1:c.447A>G NP_001166926.1:p.Lys149=
NM_001173456.1:c.426A>G NP_001166927.1:p.Lys142=
XM_011545531.1:c.561A>G XP_011543833.1:p.Lys187=
XM_011545532.1:c.561A>G XP_011543834.1:p.Lys187=
XM_017029574.2:c.540A>G XP_016885063.1:p.Lys180=
NM_000284.4:c.426A>G MANE Select NP_000275.1:p.Lys142=
NM_001173454.2:c.540A>G NP_001166925.1:p.Lys180=
NM_001173455.2:c.447A>G NP_001166926.1:p.Lys149=
NM_001173456.2:c.426A>G NP_001166927.1:p.Lys142=