Canonical Allele Identifier: CA515486489
Gene: PDHA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.19377759G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359641G>A , CM000685.2:g.19359641G>A GRCh38
NC_000023.10:g.19377759G>A , CM000685.1:g.19377759G>A GRCh37
NC_000023.9:g.19287680G>A NCBI36
NG_016781.1:g.20749G>A
NG_021184.1:g.160621C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.1182G>A ENSP00000348062.6:p.Lys394=
ENST00000379805.4:c.*853G>A ENSP00000369133.3:n.*853G>A
ENST00000417819.6:c.1245G>A ENSP00000404616.2:p.Lys415=
ENST00000423505.6:c.1275G>A ENSP00000406473.2:p.Lys425=
ENST00000481733.2:n.956G>A
ENST00000696704.1:c.*493G>A ENSP00000512823.1:n.*493G>A
ENST00000696705.1:c.*616G>A ENSP00000512824.1:n.*616G>A
ENST00000422285.7:c.1161G>A MANE Select ENSP00000394382.2:p.Lys387=
ENST00000379804.1:c.318G>A ENSP00000369132.1:p.Lys106=
ENST00000379806.9:c.1275G>A ENSP00000369134.5:p.Lys425=
ENST00000422285.6:c.1161G>A ENSP00000394382.2:p.Lys387=
ENST00000478795.1:n.600G>A
ENST00000540249.5:c.1068G>A ENSP00000440761.1:p.Lys356=
ENST00000545074.5:c.1182G>A ENSP00000438550.1:p.Lys394=
NM_000284.3:c.1161G>A NP_000275.1:p.Lys387=
NM_001173454.1:c.1275G>A NP_001166925.1:p.Lys425=
NM_001173455.1:c.1182G>A NP_001166926.1:p.Lys394=
NM_001173456.1:c.1068G>A NP_001166927.1:p.Lys356=
XM_011545531.1:c.1296G>A XP_011543833.1:p.Lys432=
XM_011545532.1:c.1203G>A XP_011543834.1:p.Lys401=
XM_017029574.2:c.1182G>A XP_016885063.1:p.Lys394=
NM_000284.4:c.1161G>A MANE Select NP_000275.1:p.Lys387=
NM_001173454.2:c.1275G>A NP_001166925.1:p.Lys425=
NM_001173455.2:c.1182G>A NP_001166926.1:p.Lys394=
NM_001173456.2:c.1068G>A NP_001166927.1:p.Lys356=