Canonical Allele Identifier: CA412394574

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373566A>G (hg19) ; chrX:g.19355448A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355448A>G , CM000685.2:g.19355448A>G	GRCh38
NC_000023.10:g.19373566A>G , CM000685.1:g.19373566A>G	GRCh37
NC_000023.9:g.19283487A>G	NCBI36
NG_016781.1:g.16556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.724A>G	ENSP00000348062.6:p.Arg242Gly
ENST00000379805.4:c.*395A>G	ENSP00000369133.3:n.*395A>G
ENST00000417819.6:c.787A>G	ENSP00000404616.2:p.Arg263Gly
ENST00000423505.6:c.817A>G	ENSP00000406473.2:p.Arg273Gly
ENST00000481733.2:n.498A>G
ENST00000696704.1:c.*35A>G	ENSP00000512823.1:n.*35A>G
ENST00000696705.1:c.*158A>G	ENSP00000512824.1:n.*158A>G
ENST00000422285.7:c.703A>G MANE Select	ENSP00000394382.2:p.Arg235Gly
ENST00000379806.9:c.817A>G	ENSP00000369134.5:p.Arg273Gly
ENST00000422285.6:c.703A>G	ENSP00000394382.2:p.Arg235Gly
ENST00000481733.1:n.131A>G
ENST00000540249.5:c.610A>G	ENSP00000440761.1:p.Arg204Gly
ENST00000545074.5:c.724A>G	ENSP00000438550.1:p.Arg242Gly
NM_000284.3:c.703A>G	NP_000275.1:p.Arg235Gly
NM_001173454.1:c.817A>G	NP_001166925.1:p.Arg273Gly
NM_001173455.1:c.724A>G	NP_001166926.1:p.Arg242Gly
NM_001173456.1:c.610A>G	NP_001166927.1:p.Arg204Gly
XM_011545531.1:c.838A>G	XP_011543833.1:p.Arg280Gly
XM_011545532.1:c.745A>G	XP_011543834.1:p.Arg249Gly
XM_017029574.2:c.724A>G	XP_016885063.1:p.Arg242Gly
NM_000284.4:c.703A>G MANE Select	NP_000275.1:p.Arg235Gly
NM_001173454.2:c.817A>G	NP_001166925.1:p.Arg273Gly
NM_001173455.2:c.724A>G	NP_001166926.1:p.Arg242Gly
NM_001173456.2:c.610A>G	NP_001166927.1:p.Arg204Gly