Canonical Allele Identifier: CA412396280

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377131G>C (hg19) ; chrX:g.19359013G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359013G>C , CM000685.2:g.19359013G>C	GRCh38
NC_000023.10:g.19377131G>C , CM000685.1:g.19377131G>C	GRCh37
NC_000023.9:g.19287052G>C	NCBI36
NG_016781.1:g.20121G>C
NG_021184.1:g.161249C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1018G>C	ENSP00000348062.6:p.Glu340Gln
ENST00000379805.4:c.*689G>C	ENSP00000369133.3:n.*689G>C
ENST00000417819.6:c.1081G>C	ENSP00000404616.2:p.Glu361Gln
ENST00000423505.6:c.1111G>C	ENSP00000406473.2:p.Glu371Gln
ENST00000481733.2:n.792G>C
ENST00000696704.1:c.*329G>C	ENSP00000512823.1:n.*329G>C
ENST00000696705.1:c.*452G>C	ENSP00000512824.1:n.*452G>C
ENST00000422285.7:c.997G>C MANE Select	ENSP00000394382.2:p.Glu333Gln
ENST00000379804.1:c.154G>C	ENSP00000369132.1:p.Glu52Gln
ENST00000379806.9:c.1111G>C	ENSP00000369134.5:p.Glu371Gln
ENST00000422285.6:c.997G>C	ENSP00000394382.2:p.Glu333Gln
ENST00000478795.1:n.436G>C
ENST00000481733.1:n.425G>C
ENST00000540249.5:c.904G>C	ENSP00000440761.1:p.Glu302Gln
ENST00000545074.5:c.1018G>C	ENSP00000438550.1:p.Glu340Gln
NM_000284.3:c.997G>C	NP_000275.1:p.Glu333Gln
NM_001173454.1:c.1111G>C	NP_001166925.1:p.Glu371Gln
NM_001173455.1:c.1018G>C	NP_001166926.1:p.Glu340Gln
NM_001173456.1:c.904G>C	NP_001166927.1:p.Glu302Gln
XM_011545531.1:c.1132G>C	XP_011543833.1:p.Glu378Gln
XM_011545532.1:c.1039G>C	XP_011543834.1:p.Glu347Gln
XM_017029574.2:c.1018G>C	XP_016885063.1:p.Glu340Gln
NM_000284.4:c.997G>C MANE Select	NP_000275.1:p.Glu333Gln
NM_001173454.2:c.1111G>C	NP_001166925.1:p.Glu371Gln
NM_001173455.2:c.1018G>C	NP_001166926.1:p.Glu340Gln
NM_001173456.2:c.904G>C	NP_001166927.1:p.Glu302Gln