Canonical Allele Identifier: CA412395231

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19375813A>T (hg19) ; chrX:g.19357695A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357695A>T , CM000685.2:g.19357695A>T	GRCh38
NC_000023.10:g.19375813A>T , CM000685.1:g.19375813A>T	GRCh37
NC_000023.9:g.19285734A>T	NCBI36
NG_016781.1:g.18803A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.896A>T	ENSP00000348062.6:p.His299Leu
ENST00000379805.4:c.*567A>T	ENSP00000369133.3:n.*567A>T
ENST00000417819.6:c.959A>T	ENSP00000404616.2:p.His320Leu
ENST00000423505.6:c.989A>T	ENSP00000406473.2:p.His330Leu
ENST00000481733.2:n.670A>T
ENST00000696704.1:c.*207A>T	ENSP00000512823.1:n.*207A>T
ENST00000696705.1:c.*330A>T	ENSP00000512824.1:n.*330A>T
ENST00000422285.7:c.875A>T MANE Select	ENSP00000394382.2:p.His292Leu
ENST00000379804.1:c.32A>T	ENSP00000369132.1:p.His11Leu
ENST00000379806.9:c.989A>T	ENSP00000369134.5:p.His330Leu
ENST00000422285.6:c.875A>T	ENSP00000394382.2:p.His292Leu
ENST00000478795.1:n.314A>T
ENST00000481733.1:n.303A>T
ENST00000540249.5:c.782A>T	ENSP00000440761.1:p.His261Leu
ENST00000545074.5:c.896A>T	ENSP00000438550.1:p.His299Leu
NM_000284.3:c.875A>T	NP_000275.1:p.His292Leu
NM_001173454.1:c.989A>T	NP_001166925.1:p.His330Leu
NM_001173455.1:c.896A>T	NP_001166926.1:p.His299Leu
NM_001173456.1:c.782A>T	NP_001166927.1:p.His261Leu
XM_011545531.1:c.1010A>T	XP_011543833.1:p.His337Leu
XM_011545532.1:c.917A>T	XP_011543834.1:p.His306Leu
XM_017029574.2:c.896A>T	XP_016885063.1:p.His299Leu
NM_000284.4:c.875A>T MANE Select	NP_000275.1:p.His292Leu
NM_001173454.2:c.989A>T	NP_001166925.1:p.His330Leu
NM_001173455.2:c.896A>T	NP_001166926.1:p.His299Leu
NM_001173456.2:c.782A>T	NP_001166927.1:p.His261Leu