Canonical Allele Identifier: CA412394522

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373542T>G (hg19) ; chrX:g.19355424T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355424T>G , CM000685.2:g.19355424T>G	GRCh38
NC_000023.10:g.19373542T>G , CM000685.1:g.19373542T>G	GRCh37
NC_000023.9:g.19283463T>G	NCBI36
NG_016781.1:g.16532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.700T>G	ENSP00000348062.6:p.Tyr234Asp
ENST00000379805.4:c.*371T>G	ENSP00000369133.3:n.*371T>G
ENST00000417819.6:c.763T>G	ENSP00000404616.2:p.Tyr255Asp
ENST00000423505.6:c.793T>G	ENSP00000406473.2:p.Tyr265Asp
ENST00000481733.2:n.474T>G
ENST00000696704.1:c.*11T>G	ENSP00000512823.1:n.*11T>G
ENST00000696705.1:c.*134T>G	ENSP00000512824.1:n.*134T>G
ENST00000422285.7:c.679T>G MANE Select	ENSP00000394382.2:p.Tyr227Asp
ENST00000379806.9:c.793T>G	ENSP00000369134.5:p.Tyr265Asp
ENST00000422285.6:c.679T>G	ENSP00000394382.2:p.Tyr227Asp
ENST00000479146.1:n.514T>G
ENST00000481733.1:n.107T>G
ENST00000540249.5:c.586T>G	ENSP00000440761.1:p.Tyr196Asp
ENST00000545074.5:c.700T>G	ENSP00000438550.1:p.Tyr234Asp
NM_000284.3:c.679T>G	NP_000275.1:p.Tyr227Asp
NM_001173454.1:c.793T>G	NP_001166925.1:p.Tyr265Asp
NM_001173455.1:c.700T>G	NP_001166926.1:p.Tyr234Asp
NM_001173456.1:c.586T>G	NP_001166927.1:p.Tyr196Asp
XM_011545531.1:c.814T>G	XP_011543833.1:p.Tyr272Asp
XM_011545532.1:c.721T>G	XP_011543834.1:p.Tyr241Asp
XM_017029574.2:c.700T>G	XP_016885063.1:p.Tyr234Asp
NM_000284.4:c.679T>G MANE Select	NP_000275.1:p.Tyr227Asp
NM_001173454.2:c.793T>G	NP_001166925.1:p.Tyr265Asp
NM_001173455.2:c.700T>G	NP_001166926.1:p.Tyr234Asp
NM_001173456.2:c.586T>G	NP_001166927.1:p.Tyr196Asp