Canonical Allele Identifier: CA412396069

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377047G>T (hg19) ; chrX:g.19358929G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358929G>T , CM000685.2:g.19358929G>T	GRCh38
NC_000023.10:g.19377047G>T , CM000685.1:g.19377047G>T	GRCh37
NC_000023.9:g.19286968G>T	NCBI36
NG_016781.1:g.20037G>T
NG_021184.1:g.161333C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.934G>T	ENSP00000348062.6:p.Glu312Ter
ENST00000379805.4:c.*605G>T	ENSP00000369133.3:n.*605G>T
ENST00000417819.6:c.997G>T	ENSP00000404616.2:p.Glu333Ter
ENST00000423505.6:c.1027G>T	ENSP00000406473.2:p.Glu343Ter
ENST00000481733.2:n.708G>T
ENST00000696704.1:c.*245G>T	ENSP00000512823.1:n.*245G>T
ENST00000696705.1:c.*368G>T	ENSP00000512824.1:n.*368G>T
ENST00000422285.7:c.913G>T MANE Select	ENSP00000394382.2:p.Glu305Ter
ENST00000379804.1:c.70G>T	ENSP00000369132.1:p.Glu24Ter
ENST00000379806.9:c.1027G>T	ENSP00000369134.5:p.Glu343Ter
ENST00000422285.6:c.913G>T	ENSP00000394382.2:p.Glu305Ter
ENST00000478795.1:n.352G>T
ENST00000481733.1:n.341G>T
ENST00000540249.5:c.820G>T	ENSP00000440761.1:p.Glu274Ter
ENST00000545074.5:c.934G>T	ENSP00000438550.1:p.Glu312Ter
NM_000284.3:c.913G>T	NP_000275.1:p.Glu305Ter
NM_001173454.1:c.1027G>T	NP_001166925.1:p.Glu343Ter
NM_001173455.1:c.934G>T	NP_001166926.1:p.Glu312Ter
NM_001173456.1:c.820G>T	NP_001166927.1:p.Glu274Ter
XM_011545531.1:c.1048G>T	XP_011543833.1:p.Glu350Ter
XM_011545532.1:c.955G>T	XP_011543834.1:p.Glu319Ter
XM_017029574.2:c.934G>T	XP_016885063.1:p.Glu312Ter
NM_000284.4:c.913G>T MANE Select	NP_000275.1:p.Glu305Ter
NM_001173454.2:c.1027G>T	NP_001166925.1:p.Glu343Ter
NM_001173455.2:c.934G>T	NP_001166926.1:p.Glu312Ter
NM_001173456.2:c.820G>T	NP_001166927.1:p.Glu274Ter