Canonical Allele Identifier: CA412394501

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373534A>T (hg19) ; chrX:g.19355416A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355416A>T , CM000685.2:g.19355416A>T	GRCh38
NC_000023.10:g.19373534A>T , CM000685.1:g.19373534A>T	GRCh37
NC_000023.9:g.19283455A>T	NCBI36
NG_016781.1:g.16524A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.692A>T	ENSP00000348062.6:p.Asn231Ile
ENST00000379805.4:c.*363A>T	ENSP00000369133.3:n.*363A>T
ENST00000417819.6:c.755A>T	ENSP00000404616.2:p.Asn252Ile
ENST00000423505.6:c.785A>T	ENSP00000406473.2:p.Asn262Ile
ENST00000481733.2:n.466A>T
ENST00000696704.1:c.*3A>T	ENSP00000512823.1:n.*3A>T
ENST00000696705.1:c.*126A>T	ENSP00000512824.1:n.*126A>T
ENST00000422285.7:c.671A>T MANE Select	ENSP00000394382.2:p.Asn224Ile
ENST00000379806.9:c.785A>T	ENSP00000369134.5:p.Asn262Ile
ENST00000422285.6:c.671A>T	ENSP00000394382.2:p.Asn224Ile
ENST00000479146.1:n.506A>T
ENST00000481733.1:n.99A>T
ENST00000540249.5:c.578A>T	ENSP00000440761.1:p.Asn193Ile
ENST00000545074.5:c.692A>T	ENSP00000438550.1:p.Asn231Ile
NM_000284.3:c.671A>T	NP_000275.1:p.Asn224Ile
NM_001173454.1:c.785A>T	NP_001166925.1:p.Asn262Ile
NM_001173455.1:c.692A>T	NP_001166926.1:p.Asn231Ile
NM_001173456.1:c.578A>T	NP_001166927.1:p.Asn193Ile
XM_011545531.1:c.806A>T	XP_011543833.1:p.Asn269Ile
XM_011545532.1:c.713A>T	XP_011543834.1:p.Asn238Ile
XM_017029574.2:c.692A>T	XP_016885063.1:p.Asn231Ile
NM_000284.4:c.671A>T MANE Select	NP_000275.1:p.Asn224Ile
NM_001173454.2:c.785A>T	NP_001166925.1:p.Asn262Ile
NM_001173455.2:c.692A>T	NP_001166926.1:p.Asn231Ile
NM_001173456.2:c.578A>T	NP_001166927.1:p.Asn193Ile