Canonical Allele Identifier: CA412394551

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373554A>G (hg19) ; chrX:g.19355436A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355436A>G , CM000685.2:g.19355436A>G	GRCh38
NC_000023.10:g.19373554A>G , CM000685.1:g.19373554A>G	GRCh37
NC_000023.9:g.19283475A>G	NCBI36
NG_016781.1:g.16544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.712A>G	ENSP00000348062.6:p.Thr238Ala
ENST00000379805.4:c.*383A>G	ENSP00000369133.3:n.*383A>G
ENST00000417819.6:c.775A>G	ENSP00000404616.2:p.Thr259Ala
ENST00000423505.6:c.805A>G	ENSP00000406473.2:p.Thr269Ala
ENST00000481733.2:n.486A>G
ENST00000696704.1:c.*23A>G	ENSP00000512823.1:n.*23A>G
ENST00000696705.1:c.*146A>G	ENSP00000512824.1:n.*146A>G
ENST00000422285.7:c.691A>G MANE Select	ENSP00000394382.2:p.Thr231Ala
ENST00000379806.9:c.805A>G	ENSP00000369134.5:p.Thr269Ala
ENST00000422285.6:c.691A>G	ENSP00000394382.2:p.Thr231Ala
ENST00000479146.1:n.526A>G
ENST00000481733.1:n.119A>G
ENST00000540249.5:c.598A>G	ENSP00000440761.1:p.Thr200Ala
ENST00000545074.5:c.712A>G	ENSP00000438550.1:p.Thr238Ala
NM_000284.3:c.691A>G	NP_000275.1:p.Thr231Ala
NM_001173454.1:c.805A>G	NP_001166925.1:p.Thr269Ala
NM_001173455.1:c.712A>G	NP_001166926.1:p.Thr238Ala
NM_001173456.1:c.598A>G	NP_001166927.1:p.Thr200Ala
XM_011545531.1:c.826A>G	XP_011543833.1:p.Thr276Ala
XM_011545532.1:c.733A>G	XP_011543834.1:p.Thr245Ala
XM_017029574.2:c.712A>G	XP_016885063.1:p.Thr238Ala
NM_000284.4:c.691A>G MANE Select	NP_000275.1:p.Thr231Ala
NM_001173454.2:c.805A>G	NP_001166925.1:p.Thr269Ala
NM_001173455.2:c.712A>G	NP_001166926.1:p.Thr238Ala
NM_001173456.2:c.598A>G	NP_001166927.1:p.Thr200Ala