Canonical Allele Identifier: CA412396567

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377653T>G (hg19) ; chrX:g.19359535T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359535T>G , CM000685.2:g.19359535T>G	GRCh38
NC_000023.10:g.19377653T>G , CM000685.1:g.19377653T>G	GRCh37
NC_000023.9:g.19287574T>G	NCBI36
NG_016781.1:g.20643T>G
NG_021184.1:g.160727A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1076T>G	ENSP00000348062.6:p.Phe359Cys
ENST00000379805.4:c.*747T>G	ENSP00000369133.3:n.*747T>G
ENST00000417819.6:c.1139T>G	ENSP00000404616.2:p.Phe380Cys
ENST00000423505.6:c.1169T>G	ENSP00000406473.2:p.Phe390Cys
ENST00000481733.2:n.850T>G
ENST00000696704.1:c.*387T>G	ENSP00000512823.1:n.*387T>G
ENST00000696705.1:c.*510T>G	ENSP00000512824.1:n.*510T>G
ENST00000422285.7:c.1055T>G MANE Select	ENSP00000394382.2:p.Phe352Cys
ENST00000379804.1:c.212T>G	ENSP00000369132.1:p.Phe71Cys
ENST00000379806.9:c.1169T>G	ENSP00000369134.5:p.Phe390Cys
ENST00000422285.6:c.1055T>G	ENSP00000394382.2:p.Phe352Cys
ENST00000478795.1:n.494T>G
ENST00000540249.5:c.962T>G	ENSP00000440761.1:p.Phe321Cys
ENST00000545074.5:c.1076T>G	ENSP00000438550.1:p.Phe359Cys
NM_000284.3:c.1055T>G	NP_000275.1:p.Phe352Cys
NM_001173454.1:c.1169T>G	NP_001166925.1:p.Phe390Cys
NM_001173455.1:c.1076T>G	NP_001166926.1:p.Phe359Cys
NM_001173456.1:c.962T>G	NP_001166927.1:p.Phe321Cys
XM_011545531.1:c.1190T>G	XP_011543833.1:p.Phe397Cys
XM_011545532.1:c.1097T>G	XP_011543834.1:p.Phe366Cys
XM_017029574.2:c.1076T>G	XP_016885063.1:p.Phe359Cys
NM_000284.4:c.1055T>G MANE Select	NP_000275.1:p.Phe352Cys
NM_001173454.2:c.1169T>G	NP_001166925.1:p.Phe390Cys
NM_001173455.2:c.1076T>G	NP_001166926.1:p.Phe359Cys
NM_001173456.2:c.962T>G	NP_001166927.1:p.Phe321Cys