Canonical Allele Identifier: CA412394443

Gene: PDHA1

Linked Data

• ClinVar Variation Id: 430118
• ClinVar RCV Id: RCV000494486
• dbSNP Id: rs1131691792
• MyVariant Identifiers: chrX:g.19373513C>T (hg19) ; chrX:g.19355395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355395C>T , CM000685.2:g.19355395C>T	GRCh38
NC_000023.10:g.19373513C>T , CM000685.1:g.19373513C>T	GRCh37
NC_000023.9:g.19283434C>T	NCBI36
NG_016781.1:g.16503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.671C>T	ENSP00000348062.6:p.Pro224Leu
ENST00000379805.4:c.*342C>T	ENSP00000369133.3:n.*342C>T
ENST00000417819.6:c.734C>T	ENSP00000404616.2:p.Pro245Leu
ENST00000423505.6:c.764C>T	ENSP00000406473.2:p.Pro255Leu
ENST00000481733.2:n.445C>T
ENST00000696704.1:c.465C>T	ENSP00000512823.1:p.Thr155=
ENST00000696705.1:c.*105C>T	ENSP00000512824.1:n.*105C>T
ENST00000422285.7:c.650C>T MANE Select	ENSP00000394382.2:p.Pro217Leu
ENST00000379806.9:c.764C>T	ENSP00000369134.5:p.Pro255Leu
ENST00000422285.6:c.650C>T	ENSP00000394382.2:p.Pro217Leu
ENST00000479146.1:n.485C>T
ENST00000481733.1:n.78C>T
ENST00000540249.5:c.557C>T	ENSP00000440761.1:p.Pro186Leu
ENST00000545074.5:c.671C>T	ENSP00000438550.1:p.Pro224Leu
NM_000284.3:c.650C>T	NP_000275.1:p.Pro217Leu
NM_001173454.1:c.764C>T	NP_001166925.1:p.Pro255Leu
NM_001173455.1:c.671C>T	NP_001166926.1:p.Pro224Leu
NM_001173456.1:c.557C>T	NP_001166927.1:p.Pro186Leu
XM_011545531.1:c.785C>T	XP_011543833.1:p.Pro262Leu
XM_011545532.1:c.692C>T	XP_011543834.1:p.Pro231Leu
XM_017029574.2:c.671C>T	XP_016885063.1:p.Pro224Leu
NM_000284.4:c.650C>T MANE Select	NP_000275.1:p.Pro217Leu
NM_001173454.2:c.764C>T	NP_001166925.1:p.Pro255Leu
NM_001173455.2:c.671C>T	NP_001166926.1:p.Pro224Leu
NM_001173456.2:c.557C>T	NP_001166927.1:p.Pro186Leu