Canonical Allele Identifier: CA412394484

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373527T>G (hg19) ; chrX:g.19355409T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355409T>G , CM000685.2:g.19355409T>G	GRCh38
NC_000023.10:g.19373527T>G , CM000685.1:g.19373527T>G	GRCh37
NC_000023.9:g.19283448T>G	NCBI36
NG_016781.1:g.16517T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.685T>G	ENSP00000348062.6:p.Cys229Gly
ENST00000379805.4:c.*356T>G	ENSP00000369133.3:n.*356T>G
ENST00000417819.6:c.748T>G	ENSP00000404616.2:p.Cys250Gly
ENST00000423505.6:c.778T>G	ENSP00000406473.2:p.Cys260Gly
ENST00000481733.2:n.459T>G
ENST00000696704.1:c.479T>G	ENSP00000512823.1:p.Leu160Arg
ENST00000696705.1:c.*119T>G	ENSP00000512824.1:n.*119T>G
ENST00000422285.7:c.664T>G MANE Select	ENSP00000394382.2:p.Cys222Gly
ENST00000379806.9:c.778T>G	ENSP00000369134.5:p.Cys260Gly
ENST00000422285.6:c.664T>G	ENSP00000394382.2:p.Cys222Gly
ENST00000479146.1:n.499T>G
ENST00000481733.1:n.92T>G
ENST00000540249.5:c.571T>G	ENSP00000440761.1:p.Cys191Gly
ENST00000545074.5:c.685T>G	ENSP00000438550.1:p.Cys229Gly
NM_000284.3:c.664T>G	NP_000275.1:p.Cys222Gly
NM_001173454.1:c.778T>G	NP_001166925.1:p.Cys260Gly
NM_001173455.1:c.685T>G	NP_001166926.1:p.Cys229Gly
NM_001173456.1:c.571T>G	NP_001166927.1:p.Cys191Gly
XM_011545531.1:c.799T>G	XP_011543833.1:p.Cys267Gly
XM_011545532.1:c.706T>G	XP_011543834.1:p.Cys236Gly
XM_017029574.2:c.685T>G	XP_016885063.1:p.Cys229Gly
NM_000284.4:c.664T>G MANE Select	NP_000275.1:p.Cys222Gly
NM_001173454.2:c.778T>G	NP_001166925.1:p.Cys260Gly
NM_001173455.2:c.685T>G	NP_001166926.1:p.Cys229Gly
NM_001173456.2:c.571T>G	NP_001166927.1:p.Cys191Gly