Canonical Allele Identifier: CA412390997

Gene: PDHA1

Linked Data

• gnomAD v4: X-19351321-C-G
• MyVariant Identifiers: chrX:g.19369439C>G (hg19) ; chrX:g.19351321C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19351321C>G , CM000685.2:g.19351321C>G	GRCh38
NC_000023.10:g.19369439C>G , CM000685.1:g.19369439C>G	GRCh37
NC_000023.9:g.19279360C>G	NCBI36
NG_016781.1:g.12429C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.353C>G	ENSP00000348062.6:p.Thr118Arg
ENST00000379805.4:c.332C>G	ENSP00000369133.3:p.Thr111Arg
ENST00000417819.6:c.416C>G	ENSP00000404616.2:p.Thr139Arg
ENST00000423505.6:c.446C>G	ENSP00000406473.2:p.Thr149Arg
ENST00000696704.1:c.332C>G	ENSP00000512823.1:p.Thr111Arg
ENST00000696705.1:c.332C>G	ENSP00000512824.1:p.Thr111Arg
ENST00000422285.7:c.332C>G MANE Select	ENSP00000394382.2:p.Thr111Arg
ENST00000355808.9:c.353C>G	ENSP00000348062.5:p.Thr118Arg
ENST00000379805.3:c.332C>G	ENSP00000369133.3:p.Thr111Arg
ENST00000379806.9:c.446C>G	ENSP00000369134.5:p.Thr149Arg
ENST00000422285.6:c.332C>G	ENSP00000394382.2:p.Thr111Arg
ENST00000423505.5:c.446C>G	ENSP00000406473.1:p.Thr149Arg
ENST00000492364.1:n.434C>G
ENST00000540249.5:c.332C>G	ENSP00000440761.1:p.Thr111Arg
ENST00000545074.5:c.353C>G	ENSP00000438550.1:p.Thr118Arg
NM_000284.3:c.332C>G	NP_000275.1:p.Thr111Arg
NM_001173454.1:c.446C>G	NP_001166925.1:p.Thr149Arg
NM_001173455.1:c.353C>G	NP_001166926.1:p.Thr118Arg
NM_001173456.1:c.332C>G	NP_001166927.1:p.Thr111Arg
XM_011545531.1:c.467C>G	XP_011543833.1:p.Thr156Arg
XM_011545532.1:c.467C>G	XP_011543834.1:p.Thr156Arg
XM_017029574.2:c.446C>G	XP_016885063.1:p.Thr149Arg
NM_000284.4:c.332C>G MANE Select	NP_000275.1:p.Thr111Arg
NM_001173454.2:c.446C>G	NP_001166925.1:p.Thr149Arg
NM_001173455.2:c.353C>G	NP_001166926.1:p.Thr118Arg
NM_001173456.2:c.332C>G	NP_001166927.1:p.Thr111Arg