Canonical Allele Identifier: CA412394562

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373560G>T (hg19) ; chrX:g.19355442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355442G>T , CM000685.2:g.19355442G>T	GRCh38
NC_000023.10:g.19373560G>T , CM000685.1:g.19373560G>T	GRCh37
NC_000023.9:g.19283481G>T	NCBI36
NG_016781.1:g.16550G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.718G>T	ENSP00000348062.6:p.Val240Phe
ENST00000379805.4:c.*389G>T	ENSP00000369133.3:n.*389G>T
ENST00000417819.6:c.781G>T	ENSP00000404616.2:p.Val261Phe
ENST00000423505.6:c.811G>T	ENSP00000406473.2:p.Val271Phe
ENST00000481733.2:n.492G>T
ENST00000696704.1:c.*29G>T	ENSP00000512823.1:n.*29G>T
ENST00000696705.1:c.*152G>T	ENSP00000512824.1:n.*152G>T
ENST00000422285.7:c.697G>T MANE Select	ENSP00000394382.2:p.Val233Phe
ENST00000379806.9:c.811G>T	ENSP00000369134.5:p.Val271Phe
ENST00000422285.6:c.697G>T	ENSP00000394382.2:p.Val233Phe
ENST00000479146.1:n.532G>T
ENST00000481733.1:n.125G>T
ENST00000540249.5:c.604G>T	ENSP00000440761.1:p.Val202Phe
ENST00000545074.5:c.718G>T	ENSP00000438550.1:p.Val240Phe
NM_000284.3:c.697G>T	NP_000275.1:p.Val233Phe
NM_001173454.1:c.811G>T	NP_001166925.1:p.Val271Phe
NM_001173455.1:c.718G>T	NP_001166926.1:p.Val240Phe
NM_001173456.1:c.604G>T	NP_001166927.1:p.Val202Phe
XM_011545531.1:c.832G>T	XP_011543833.1:p.Val278Phe
XM_011545532.1:c.739G>T	XP_011543834.1:p.Val247Phe
XM_017029574.2:c.718G>T	XP_016885063.1:p.Val240Phe
NM_000284.4:c.697G>T MANE Select	NP_000275.1:p.Val233Phe
NM_001173454.2:c.811G>T	NP_001166925.1:p.Val271Phe
NM_001173455.2:c.718G>T	NP_001166926.1:p.Val240Phe
NM_001173456.2:c.604G>T	NP_001166927.1:p.Val202Phe