Canonical Allele Identifier: CA515486292

Gene: PDHA1

Linked Data

• gnomAD v4: X-19358934-A-G
• MyVariant Identifiers: chrX:g.19377052A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358934A>G , CM000685.2:g.19358934A>G	GRCh38
NC_000023.10:g.19377052A>G , CM000685.1:g.19377052A>G	GRCh37
NC_000023.9:g.19286973A>G	NCBI36
NG_016781.1:g.20042A>G
NG_021184.1:g.161328T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.939A>G	ENSP00000348062.6:p.Glu313=
ENST00000379805.4:c.*610A>G	ENSP00000369133.3:n.*610A>G
ENST00000417819.6:c.1002A>G	ENSP00000404616.2:p.Glu334=
ENST00000423505.6:c.1032A>G	ENSP00000406473.2:p.Glu344=
ENST00000481733.2:n.713A>G
ENST00000696704.1:c.*250A>G	ENSP00000512823.1:n.*250A>G
ENST00000696705.1:c.*373A>G	ENSP00000512824.1:n.*373A>G
ENST00000422285.7:c.918A>G MANE Select	ENSP00000394382.2:p.Glu306=
ENST00000379804.1:c.75A>G	ENSP00000369132.1:p.Glu25=
ENST00000379806.9:c.1032A>G	ENSP00000369134.5:p.Glu344=
ENST00000422285.6:c.918A>G	ENSP00000394382.2:p.Glu306=
ENST00000478795.1:n.357A>G
ENST00000481733.1:n.346A>G
ENST00000540249.5:c.825A>G	ENSP00000440761.1:p.Glu275=
ENST00000545074.5:c.939A>G	ENSP00000438550.1:p.Glu313=
NM_000284.3:c.918A>G	NP_000275.1:p.Glu306=
NM_001173454.1:c.1032A>G	NP_001166925.1:p.Glu344=
NM_001173455.1:c.939A>G	NP_001166926.1:p.Glu313=
NM_001173456.1:c.825A>G	NP_001166927.1:p.Glu275=
XM_011545531.1:c.1053A>G	XP_011543833.1:p.Glu351=
XM_011545532.1:c.960A>G	XP_011543834.1:p.Glu320=
XM_017029574.2:c.939A>G	XP_016885063.1:p.Glu313=
NM_000284.4:c.918A>G MANE Select	NP_000275.1:p.Glu306=
NM_001173454.2:c.1032A>G	NP_001166925.1:p.Glu344=
NM_001173455.2:c.939A>G	NP_001166926.1:p.Glu313=
NM_001173456.2:c.825A>G	NP_001166927.1:p.Glu275=