Canonical Allele Identifier: CA412394563

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373561T>A (hg19) ; chrX:g.19355443T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355443T>A , CM000685.2:g.19355443T>A	GRCh38
NC_000023.10:g.19373561T>A , CM000685.1:g.19373561T>A	GRCh37
NC_000023.9:g.19283482T>A	NCBI36
NG_016781.1:g.16551T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.719T>A	ENSP00000348062.6:p.Val240Asp
ENST00000379805.4:c.*390T>A	ENSP00000369133.3:n.*390T>A
ENST00000417819.6:c.782T>A	ENSP00000404616.2:p.Val261Asp
ENST00000423505.6:c.812T>A	ENSP00000406473.2:p.Val271Asp
ENST00000481733.2:n.493T>A
ENST00000696704.1:c.*30T>A	ENSP00000512823.1:n.*30T>A
ENST00000696705.1:c.*153T>A	ENSP00000512824.1:n.*153T>A
ENST00000422285.7:c.698T>A MANE Select	ENSP00000394382.2:p.Val233Asp
ENST00000379806.9:c.812T>A	ENSP00000369134.5:p.Val271Asp
ENST00000422285.6:c.698T>A	ENSP00000394382.2:p.Val233Asp
ENST00000479146.1:n.533T>A
ENST00000481733.1:n.126T>A
ENST00000540249.5:c.605T>A	ENSP00000440761.1:p.Val202Asp
ENST00000545074.5:c.719T>A	ENSP00000438550.1:p.Val240Asp
NM_000284.3:c.698T>A	NP_000275.1:p.Val233Asp
NM_001173454.1:c.812T>A	NP_001166925.1:p.Val271Asp
NM_001173455.1:c.719T>A	NP_001166926.1:p.Val240Asp
NM_001173456.1:c.605T>A	NP_001166927.1:p.Val202Asp
XM_011545531.1:c.833T>A	XP_011543833.1:p.Val278Asp
XM_011545532.1:c.740T>A	XP_011543834.1:p.Val247Asp
XM_017029574.2:c.719T>A	XP_016885063.1:p.Val240Asp
NM_000284.4:c.698T>A MANE Select	NP_000275.1:p.Val233Asp
NM_001173454.2:c.812T>A	NP_001166925.1:p.Val271Asp
NM_001173455.2:c.719T>A	NP_001166926.1:p.Val240Asp
NM_001173456.2:c.605T>A	NP_001166927.1:p.Val202Asp