Canonical Allele Identifier: CA412396084

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377050G>A (hg19) ; chrX:g.19358932G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358932G>A , CM000685.2:g.19358932G>A	GRCh38
NC_000023.10:g.19377050G>A , CM000685.1:g.19377050G>A	GRCh37
NC_000023.9:g.19286971G>A	NCBI36
NG_016781.1:g.20040G>A
NG_021184.1:g.161330C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.937G>A	ENSP00000348062.6:p.Glu313Lys
ENST00000379805.4:c.*608G>A	ENSP00000369133.3:n.*608G>A
ENST00000417819.6:c.1000G>A	ENSP00000404616.2:p.Glu334Lys
ENST00000423505.6:c.1030G>A	ENSP00000406473.2:p.Glu344Lys
ENST00000481733.2:n.711G>A
ENST00000696704.1:c.*248G>A	ENSP00000512823.1:n.*248G>A
ENST00000696705.1:c.*371G>A	ENSP00000512824.1:n.*371G>A
ENST00000422285.7:c.916G>A MANE Select	ENSP00000394382.2:p.Glu306Lys
ENST00000379804.1:c.73G>A	ENSP00000369132.1:p.Glu25Lys
ENST00000379806.9:c.1030G>A	ENSP00000369134.5:p.Glu344Lys
ENST00000422285.6:c.916G>A	ENSP00000394382.2:p.Glu306Lys
ENST00000478795.1:n.355G>A
ENST00000481733.1:n.344G>A
ENST00000540249.5:c.823G>A	ENSP00000440761.1:p.Glu275Lys
ENST00000545074.5:c.937G>A	ENSP00000438550.1:p.Glu313Lys
NM_000284.3:c.916G>A	NP_000275.1:p.Glu306Lys
NM_001173454.1:c.1030G>A	NP_001166925.1:p.Glu344Lys
NM_001173455.1:c.937G>A	NP_001166926.1:p.Glu313Lys
NM_001173456.1:c.823G>A	NP_001166927.1:p.Glu275Lys
XM_011545531.1:c.1051G>A	XP_011543833.1:p.Glu351Lys
XM_011545532.1:c.958G>A	XP_011543834.1:p.Glu320Lys
XM_017029574.2:c.937G>A	XP_016885063.1:p.Glu313Lys
NM_000284.4:c.916G>A MANE Select	NP_000275.1:p.Glu306Lys
NM_001173454.2:c.1030G>A	NP_001166925.1:p.Glu344Lys
NM_001173455.2:c.937G>A	NP_001166926.1:p.Glu313Lys
NM_001173456.2:c.823G>A	NP_001166927.1:p.Glu275Lys