Canonical Allele Identifier: CA412394581

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373569G>A (hg19) ; chrX:g.19355451G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355451G>A , CM000685.2:g.19355451G>A	GRCh38
NC_000023.10:g.19373569G>A , CM000685.1:g.19373569G>A	GRCh37
NC_000023.9:g.19283490G>A	NCBI36
NG_016781.1:g.16559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.727G>A	ENSP00000348062.6:p.Ala243Thr
ENST00000379805.4:c.*398G>A	ENSP00000369133.3:n.*398G>A
ENST00000417819.6:c.790G>A	ENSP00000404616.2:p.Ala264Thr
ENST00000423505.6:c.820G>A	ENSP00000406473.2:p.Ala274Thr
ENST00000481733.2:n.501G>A
ENST00000696704.1:c.*38G>A	ENSP00000512823.1:n.*38G>A
ENST00000696705.1:c.*161G>A	ENSP00000512824.1:n.*161G>A
ENST00000422285.7:c.706G>A MANE Select	ENSP00000394382.2:p.Ala236Thr
ENST00000379806.9:c.820G>A	ENSP00000369134.5:p.Ala274Thr
ENST00000422285.6:c.706G>A	ENSP00000394382.2:p.Ala236Thr
ENST00000481733.1:n.134G>A
ENST00000540249.5:c.613G>A	ENSP00000440761.1:p.Ala205Thr
ENST00000545074.5:c.727G>A	ENSP00000438550.1:p.Ala243Thr
NM_000284.3:c.706G>A	NP_000275.1:p.Ala236Thr
NM_001173454.1:c.820G>A	NP_001166925.1:p.Ala274Thr
NM_001173455.1:c.727G>A	NP_001166926.1:p.Ala243Thr
NM_001173456.1:c.613G>A	NP_001166927.1:p.Ala205Thr
XM_011545531.1:c.841G>A	XP_011543833.1:p.Ala281Thr
XM_011545532.1:c.748G>A	XP_011543834.1:p.Ala250Thr
XM_017029574.2:c.727G>A	XP_016885063.1:p.Ala243Thr
NM_000284.4:c.706G>A MANE Select	NP_000275.1:p.Ala236Thr
NM_001173454.2:c.820G>A	NP_001166925.1:p.Ala274Thr
NM_001173455.2:c.727G>A	NP_001166926.1:p.Ala243Thr
NM_001173456.2:c.613G>A	NP_001166927.1:p.Ala205Thr