Canonical Allele Identifier: CA515485986

Gene: PDHA1

Linked Data

• COSMIC: COSM375263
• MyVariant Identifiers: chrX:g.19373472G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355354G>A , CM000685.2:g.19355354G>A	GRCh38
NC_000023.10:g.19373472G>A , CM000685.1:g.19373472G>A	GRCh37
NC_000023.9:g.19283393G>A	NCBI36
NG_016781.1:g.16462G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.630G>A	ENSP00000348062.6:p.Gln210=
ENST00000379805.4:c.*301G>A	ENSP00000369133.3:n.*301G>A
ENST00000417819.6:c.693G>A	ENSP00000404616.2:p.Gln231=
ENST00000423505.6:c.723G>A	ENSP00000406473.2:p.Gln241=
ENST00000481733.2:n.404G>A
ENST00000696704.1:c.424G>A	ENSP00000512823.1:p.Asp142Asn
ENST00000696705.1:c.*64G>A	ENSP00000512824.1:n.*64G>A
ENST00000422285.7:c.609G>A MANE Select	ENSP00000394382.2:p.Gln203=
ENST00000379806.9:c.723G>A	ENSP00000369134.5:p.Gln241=
ENST00000422285.6:c.609G>A	ENSP00000394382.2:p.Gln203=
ENST00000479146.1:n.444G>A
ENST00000481733.1:n.37G>A
ENST00000540249.5:c.516G>A	ENSP00000440761.1:p.Gln172=
ENST00000545074.5:c.630G>A	ENSP00000438550.1:p.Gln210=
NM_000284.3:c.609G>A	NP_000275.1:p.Gln203=
NM_001173454.1:c.723G>A	NP_001166925.1:p.Gln241=
NM_001173455.1:c.630G>A	NP_001166926.1:p.Gln210=
NM_001173456.1:c.516G>A	NP_001166927.1:p.Gln172=
XM_011545531.1:c.744G>A	XP_011543833.1:p.Gln248=
XM_011545532.1:c.651G>A	XP_011543834.1:p.Gln217=
XM_017029574.2:c.630G>A	XP_016885063.1:p.Gln210=
NM_000284.4:c.609G>A MANE Select	NP_000275.1:p.Gln203=
NM_001173454.2:c.723G>A	NP_001166925.1:p.Gln241=
NM_001173455.2:c.630G>A	NP_001166926.1:p.Gln210=
NM_001173456.2:c.516G>A	NP_001166927.1:p.Gln172=