Canonical Allele Identifier: CA412397324

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377755T>A (hg19) ; chrX:g.19359637T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359637T>A , CM000685.2:g.19359637T>A	GRCh38
NC_000023.10:g.19377755T>A , CM000685.1:g.19377755T>A	GRCh37
NC_000023.9:g.19287676T>A	NCBI36
NG_016781.1:g.20745T>A
NG_021184.1:g.160625A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1178T>A	ENSP00000348062.6:p.Phe393Tyr
ENST00000379805.4:c.*849T>A	ENSP00000369133.3:n.*849T>A
ENST00000417819.6:c.1241T>A	ENSP00000404616.2:p.Phe414Tyr
ENST00000423505.6:c.1271T>A	ENSP00000406473.2:p.Phe424Tyr
ENST00000481733.2:n.952T>A
ENST00000696704.1:c.*489T>A	ENSP00000512823.1:n.*489T>A
ENST00000696705.1:c.*612T>A	ENSP00000512824.1:n.*612T>A
ENST00000422285.7:c.1157T>A MANE Select	ENSP00000394382.2:p.Phe386Tyr
ENST00000379804.1:c.314T>A	ENSP00000369132.1:p.Phe105Tyr
ENST00000379806.9:c.1271T>A	ENSP00000369134.5:p.Phe424Tyr
ENST00000422285.6:c.1157T>A	ENSP00000394382.2:p.Phe386Tyr
ENST00000478795.1:n.596T>A
ENST00000540249.5:c.1064T>A	ENSP00000440761.1:p.Phe355Tyr
ENST00000545074.5:c.1178T>A	ENSP00000438550.1:p.Phe393Tyr
NM_000284.3:c.1157T>A	NP_000275.1:p.Phe386Tyr
NM_001173454.1:c.1271T>A	NP_001166925.1:p.Phe424Tyr
NM_001173455.1:c.1178T>A	NP_001166926.1:p.Phe393Tyr
NM_001173456.1:c.1064T>A	NP_001166927.1:p.Phe355Tyr
XM_011545531.1:c.1292T>A	XP_011543833.1:p.Phe431Tyr
XM_011545532.1:c.1199T>A	XP_011543834.1:p.Phe400Tyr
XM_017029574.2:c.1178T>A	XP_016885063.1:p.Phe393Tyr
NM_000284.4:c.1157T>A MANE Select	NP_000275.1:p.Phe386Tyr
NM_001173454.2:c.1271T>A	NP_001166925.1:p.Phe424Tyr
NM_001173455.2:c.1178T>A	NP_001166926.1:p.Phe393Tyr
NM_001173456.2:c.1064T>A	NP_001166927.1:p.Phe355Tyr