Canonical Allele Identifier: CA2693250543

Gene: PDHA1

Linked Data

• gnomAD v4: X-19355666-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355666C>T , CM000685.2:g.19355666C>T	GRCh38
NC_000023.10:g.19373784C>T , CM000685.1:g.19373784C>T	GRCh37
NC_000023.9:g.19283705C>T	NCBI36
NG_016781.1:g.16774C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.781-20C>T	ENSP00000348062.6:n.781-20C>T
ENST00000379805.4:c.*452-20C>T	ENSP00000369133.3:n.*452-20C>T
ENST00000417819.6:c.844-20C>T	ENSP00000404616.2:n.844-20C>T
ENST00000423505.6:c.874-20C>T	ENSP00000406473.2:n.874-20C>T
ENST00000481733.2:n.555-20C>T
ENST00000696704.1:c.*92-20C>T	ENSP00000512823.1:n.*92-20C>T
ENST00000696705.1:c.*215-20C>T	ENSP00000512824.1:n.*215-20C>T
ENST00000422285.7:c.760-20C>T MANE Select	ENSP00000394382.2:n.760-20C>T
ENST00000379804.1:c.-104C>T	ENSP00000369132.1:n.-104C>T
ENST00000379806.9:c.874-20C>T	ENSP00000369134.5:n.874-20C>T
ENST00000422285.6:c.760-20C>T	ENSP00000394382.2:n.760-20C>T
ENST00000481733.1:n.188-20C>T
ENST00000540249.5:c.667-20C>T	ENSP00000440761.1:n.667-20C>T
ENST00000545074.5:c.781-20C>T	ENSP00000438550.1:n.781-20C>T
NM_000284.3:c.760-20C>T	NP_000275.1:n.760-20C>T
NM_001173454.1:c.874-20C>T	NP_001166925.1:n.874-20C>T
NM_001173455.1:c.781-20C>T	NP_001166926.1:n.781-20C>T
NM_001173456.1:c.667-20C>T	NP_001166927.1:n.667-20C>T
XM_011545531.1:c.895-20C>T	XP_011543833.1:n.895-20C>T
XM_011545532.1:c.802-20C>T	XP_011543834.1:n.802-20C>T
XM_017029574.2:c.781-20C>T	XP_016885063.1:n.781-20C>T
NM_000284.4:c.760-20C>T MANE Select	NP_000275.1:n.760-20C>T
NM_001173454.2:c.874-20C>T	NP_001166925.1:n.874-20C>T
NM_001173455.2:c.781-20C>T	NP_001166926.1:n.781-20C>T
NM_001173456.2:c.667-20C>T	NP_001166927.1:n.667-20C>T