Canonical Allele Identifier: CA412394230

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373470C>G (hg19) ; chrX:g.19355352C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355352C>G , CM000685.2:g.19355352C>G	GRCh38
NC_000023.10:g.19373470C>G , CM000685.1:g.19373470C>G	GRCh37
NC_000023.9:g.19283391C>G	NCBI36
NG_016781.1:g.16460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.628C>G	ENSP00000348062.6:p.Gln210Glu
ENST00000379805.4:c.*299C>G	ENSP00000369133.3:n.*299C>G
ENST00000417819.6:c.691C>G	ENSP00000404616.2:p.Gln231Glu
ENST00000423505.6:c.721C>G	ENSP00000406473.2:p.Gln241Glu
ENST00000481733.2:n.402C>G
ENST00000696704.1:c.422C>G	ENSP00000512823.1:p.Pro141Arg
ENST00000696705.1:c.*62C>G	ENSP00000512824.1:n.*62C>G
ENST00000422285.7:c.607C>G MANE Select	ENSP00000394382.2:p.Gln203Glu
ENST00000379806.9:c.721C>G	ENSP00000369134.5:p.Gln241Glu
ENST00000422285.6:c.607C>G	ENSP00000394382.2:p.Gln203Glu
ENST00000479146.1:n.442C>G
ENST00000481733.1:n.35C>G
ENST00000540249.5:c.514C>G	ENSP00000440761.1:p.Gln172Glu
ENST00000545074.5:c.628C>G	ENSP00000438550.1:p.Gln210Glu
NM_000284.3:c.607C>G	NP_000275.1:p.Gln203Glu
NM_001173454.1:c.721C>G	NP_001166925.1:p.Gln241Glu
NM_001173455.1:c.628C>G	NP_001166926.1:p.Gln210Glu
NM_001173456.1:c.514C>G	NP_001166927.1:p.Gln172Glu
XM_011545531.1:c.742C>G	XP_011543833.1:p.Gln248Glu
XM_011545532.1:c.649C>G	XP_011543834.1:p.Gln217Glu
XM_017029574.2:c.628C>G	XP_016885063.1:p.Gln210Glu
NM_000284.4:c.607C>G MANE Select	NP_000275.1:p.Gln203Glu
NM_001173454.2:c.721C>G	NP_001166925.1:p.Gln241Glu
NM_001173455.2:c.628C>G	NP_001166926.1:p.Gln210Glu
NM_001173456.2:c.514C>G	NP_001166927.1:p.Gln172Glu