Canonical Allele Identifier: CA515485909

Gene: PDHA1

Linked Data

• gnomAD v4: X-19353170-G-T
• COSMIC: COSM756600 ; COSM1648271
• MyVariant Identifiers: chrX:g.19371288G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19353170G>T , CM000685.2:g.19353170G>T	GRCh38
NC_000023.10:g.19371288G>T , CM000685.1:g.19371288G>T	GRCh37
NC_000023.9:g.19281209G>T	NCBI36
NG_016781.1:g.14278G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.528G>T	ENSP00000348062.6:p.Ala176=
ENST00000379805.4:c.507G>T	ENSP00000369133.3:p.Ala169=
ENST00000417819.6:c.591G>T	ENSP00000404616.2:p.Ala197=
ENST00000423505.6:c.621G>T	ENSP00000406473.2:p.Ala207=
ENST00000696704.1:c.418+1763G>T	ENSP00000512823.1:n.418+1763G>T
ENST00000696705.1:c.419-1321G>T	ENSP00000512824.1:n.419-1321G>T
ENST00000422285.7:c.507G>T MANE Select	ENSP00000394382.2:p.Ala169=
ENST00000355808.9:c.528G>T	ENSP00000348062.5:p.Ala176=
ENST00000379805.3:c.507G>T	ENSP00000369133.3:p.Ala169=
ENST00000379806.9:c.621G>T	ENSP00000369134.5:p.Ala207=
ENST00000422285.6:c.507G>T	ENSP00000394382.2:p.Ala169=
ENST00000479146.1:n.342G>T
ENST00000540249.5:c.507G>T	ENSP00000440761.1:p.Ala169=
ENST00000545074.5:c.528G>T	ENSP00000438550.1:p.Ala176=
NM_000284.3:c.507G>T	NP_000275.1:p.Ala169=
NM_001173454.1:c.621G>T	NP_001166925.1:p.Ala207=
NM_001173455.1:c.528G>T	NP_001166926.1:p.Ala176=
NM_001173456.1:c.507G>T	NP_001166927.1:p.Ala169=
XM_011545531.1:c.642G>T	XP_011543833.1:p.Ala214=
XM_011545532.1:c.642G>T	XP_011543834.1:p.Ala214=
XM_017029574.2:c.621G>T	XP_016885063.1:p.Ala207=
NM_000284.4:c.507G>T MANE Select	NP_000275.1:p.Ala169=
NM_001173454.2:c.621G>T	NP_001166925.1:p.Ala207=
NM_001173455.2:c.528G>T	NP_001166926.1:p.Ala176=
NM_001173456.2:c.507G>T	NP_001166927.1:p.Ala169=