Canonical Allele Identifier: CA515486146

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19375775C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357657C>A , CM000685.2:g.19357657C>A	GRCh38
NC_000023.10:g.19375775C>A , CM000685.1:g.19375775C>A	GRCh37
NC_000023.9:g.19285696C>A	NCBI36
NG_016781.1:g.18765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.858C>A	ENSP00000348062.6:p.Pro286=
ENST00000379805.4:c.*529C>A	ENSP00000369133.3:n.*529C>A
ENST00000417819.6:c.921C>A	ENSP00000404616.2:p.Pro307=
ENST00000423505.6:c.951C>A	ENSP00000406473.2:p.Pro317=
ENST00000481733.2:n.632C>A
ENST00000696704.1:c.*169C>A	ENSP00000512823.1:n.*169C>A
ENST00000696705.1:c.*292C>A	ENSP00000512824.1:n.*292C>A
ENST00000422285.7:c.837C>A MANE Select	ENSP00000394382.2:p.Pro279=
ENST00000379804.1:c.-7C>A	ENSP00000369132.1:n.-7C>A
ENST00000379806.9:c.951C>A	ENSP00000369134.5:p.Pro317=
ENST00000422285.6:c.837C>A	ENSP00000394382.2:p.Pro279=
ENST00000478795.1:n.276C>A
ENST00000481733.1:n.265C>A
ENST00000540249.5:c.744C>A	ENSP00000440761.1:p.Pro248=
ENST00000545074.5:c.858C>A	ENSP00000438550.1:p.Pro286=
NM_000284.3:c.837C>A	NP_000275.1:p.Pro279=
NM_001173454.1:c.951C>A	NP_001166925.1:p.Pro317=
NM_001173455.1:c.858C>A	NP_001166926.1:p.Pro286=
NM_001173456.1:c.744C>A	NP_001166927.1:p.Pro248=
XM_011545531.1:c.972C>A	XP_011543833.1:p.Pro324=
XM_011545532.1:c.879C>A	XP_011543834.1:p.Pro293=
XM_017029574.2:c.858C>A	XP_016885063.1:p.Pro286=
NM_000284.4:c.837C>A MANE Select	NP_000275.1:p.Pro279=
NM_001173454.2:c.951C>A	NP_001166925.1:p.Pro317=
NM_001173455.2:c.858C>A	NP_001166926.1:p.Pro286=
NM_001173456.2:c.744C>A	NP_001166927.1:p.Pro248=