Canonical Allele Identifier: CA412395188

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19375795C>A (hg19) ; chrX:g.19357677C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357677C>A , CM000685.2:g.19357677C>A	GRCh38
NC_000023.10:g.19375795C>A , CM000685.1:g.19375795C>A	GRCh37
NC_000023.9:g.19285716C>A	NCBI36
NG_016781.1:g.18785C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.878C>A	ENSP00000348062.6:p.Thr293Asn
ENST00000379805.4:c.*549C>A	ENSP00000369133.3:n.*549C>A
ENST00000417819.6:c.941C>A	ENSP00000404616.2:p.Thr314Asn
ENST00000423505.6:c.971C>A	ENSP00000406473.2:p.Thr324Asn
ENST00000481733.2:n.652C>A
ENST00000696704.1:c.*189C>A	ENSP00000512823.1:n.*189C>A
ENST00000696705.1:c.*312C>A	ENSP00000512824.1:n.*312C>A
ENST00000422285.7:c.857C>A MANE Select	ENSP00000394382.2:p.Thr286Asn
ENST00000379804.1:c.14C>A	ENSP00000369132.1:p.Thr5Asn
ENST00000379806.9:c.971C>A	ENSP00000369134.5:p.Thr324Asn
ENST00000422285.6:c.857C>A	ENSP00000394382.2:p.Thr286Asn
ENST00000478795.1:n.296C>A
ENST00000481733.1:n.285C>A
ENST00000540249.5:c.764C>A	ENSP00000440761.1:p.Thr255Asn
ENST00000545074.5:c.878C>A	ENSP00000438550.1:p.Thr293Asn
NM_000284.3:c.857C>A	NP_000275.1:p.Thr286Asn
NM_001173454.1:c.971C>A	NP_001166925.1:p.Thr324Asn
NM_001173455.1:c.878C>A	NP_001166926.1:p.Thr293Asn
NM_001173456.1:c.764C>A	NP_001166927.1:p.Thr255Asn
XM_011545531.1:c.992C>A	XP_011543833.1:p.Thr331Asn
XM_011545532.1:c.899C>A	XP_011543834.1:p.Thr300Asn
XM_017029574.2:c.878C>A	XP_016885063.1:p.Thr293Asn
NM_000284.4:c.857C>A MANE Select	NP_000275.1:p.Thr286Asn
NM_001173454.2:c.971C>A	NP_001166925.1:p.Thr324Asn
NM_001173455.2:c.878C>A	NP_001166926.1:p.Thr293Asn
NM_001173456.2:c.764C>A	NP_001166927.1:p.Thr255Asn