Canonical Allele Identifier: CA412396466

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377632A>T (hg19) ; chrX:g.19359514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359514A>T , CM000685.2:g.19359514A>T	GRCh38
NC_000023.10:g.19377632A>T , CM000685.1:g.19377632A>T	GRCh37
NC_000023.9:g.19287553A>T	NCBI36
NG_016781.1:g.20622A>T
NG_021184.1:g.160748T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1055A>T	ENSP00000348062.6:p.Glu352Val
ENST00000379805.4:c.*726A>T	ENSP00000369133.3:n.*726A>T
ENST00000417819.6:c.1118A>T	ENSP00000404616.2:p.Glu373Val
ENST00000423505.6:c.1148A>T	ENSP00000406473.2:p.Glu383Val
ENST00000481733.2:n.829A>T
ENST00000696704.1:c.*366A>T	ENSP00000512823.1:n.*366A>T
ENST00000696705.1:c.*489A>T	ENSP00000512824.1:n.*489A>T
ENST00000422285.7:c.1034A>T MANE Select	ENSP00000394382.2:p.Glu345Val
ENST00000379804.1:c.191A>T	ENSP00000369132.1:p.Glu64Val
ENST00000379806.9:c.1148A>T	ENSP00000369134.5:p.Glu383Val
ENST00000422285.6:c.1034A>T	ENSP00000394382.2:p.Glu345Val
ENST00000478795.1:n.473A>T
ENST00000540249.5:c.941A>T	ENSP00000440761.1:p.Glu314Val
ENST00000545074.5:c.1055A>T	ENSP00000438550.1:p.Glu352Val
NM_000284.3:c.1034A>T	NP_000275.1:p.Glu345Val
NM_001173454.1:c.1148A>T	NP_001166925.1:p.Glu383Val
NM_001173455.1:c.1055A>T	NP_001166926.1:p.Glu352Val
NM_001173456.1:c.941A>T	NP_001166927.1:p.Glu314Val
XM_011545531.1:c.1169A>T	XP_011543833.1:p.Glu390Val
XM_011545532.1:c.1076A>T	XP_011543834.1:p.Glu359Val
XM_017029574.2:c.1055A>T	XP_016885063.1:p.Glu352Val
NM_000284.4:c.1034A>T MANE Select	NP_000275.1:p.Glu345Val
NM_001173454.2:c.1148A>T	NP_001166925.1:p.Glu383Val
NM_001173455.2:c.1055A>T	NP_001166926.1:p.Glu352Val
NM_001173456.2:c.941A>T	NP_001166927.1:p.Glu314Val