Canonical Allele Identifier: CA412394678

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373611C>A (hg19) ; chrX:g.19355493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355493C>A , CM000685.2:g.19355493C>A	GRCh38
NC_000023.10:g.19373611C>A , CM000685.1:g.19373611C>A	GRCh37
NC_000023.9:g.19283532C>A	NCBI36
NG_016781.1:g.16601C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.769C>A	ENSP00000348062.6:p.Pro257Thr
ENST00000379805.4:c.*440C>A	ENSP00000369133.3:n.*440C>A
ENST00000417819.6:c.832C>A	ENSP00000404616.2:p.Pro278Thr
ENST00000423505.6:c.862C>A	ENSP00000406473.2:p.Pro288Thr
ENST00000481733.2:n.543C>A
ENST00000696704.1:c.*80C>A	ENSP00000512823.1:n.*80C>A
ENST00000696705.1:c.*203C>A	ENSP00000512824.1:n.*203C>A
ENST00000422285.7:c.748C>A MANE Select	ENSP00000394382.2:p.Pro250Thr
ENST00000379806.9:c.862C>A	ENSP00000369134.5:p.Pro288Thr
ENST00000422285.6:c.748C>A	ENSP00000394382.2:p.Pro250Thr
ENST00000481733.1:n.176C>A
ENST00000540249.5:c.655C>A	ENSP00000440761.1:p.Pro219Thr
ENST00000545074.5:c.769C>A	ENSP00000438550.1:p.Pro257Thr
NM_000284.3:c.748C>A	NP_000275.1:p.Pro250Thr
NM_001173454.1:c.862C>A	NP_001166925.1:p.Pro288Thr
NM_001173455.1:c.769C>A	NP_001166926.1:p.Pro257Thr
NM_001173456.1:c.655C>A	NP_001166927.1:p.Pro219Thr
XM_011545531.1:c.883C>A	XP_011543833.1:p.Pro295Thr
XM_011545532.1:c.790C>A	XP_011543834.1:p.Pro264Thr
XM_017029574.2:c.769C>A	XP_016885063.1:p.Pro257Thr
NM_000284.4:c.748C>A MANE Select	NP_000275.1:p.Pro250Thr
NM_001173454.2:c.862C>A	NP_001166925.1:p.Pro288Thr
NM_001173455.2:c.769C>A	NP_001166926.1:p.Pro257Thr
NM_001173456.2:c.655C>A	NP_001166927.1:p.Pro219Thr