Canonical Allele Identifier: CA380120865

Gene: PDHX

Linked Data

• MyVariant Identifiers: chr11:g.34988342C>G (hg19) ; chr11:g.34966795C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34966795C>G , CM000673.2:g.34966795C>G	GRCh38
NC_000011.9:g.34988342C>G , CM000673.1:g.34988342C>G	GRCh37
NC_000011.8:g.34944918C>G	NCBI36
NG_013368.1:g.55666C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000448838.8:c.617C>G	ENSP00000389404.3:p.Pro206Arg
ENST00000227868.9:c.797C>G MANE Select	ENSP00000227868.4:p.Pro266Arg
ENST00000227868.8:c.797C>G	ENSP00000227868.4:p.Pro266Arg
ENST00000430469.6:c.343-17775C>G	ENSP00000415695.2:n.343-17775C>G
ENST00000448838.7:c.752C>G	ENSP00000389404.2:p.Pro251Arg
NM_001135024.1:c.752C>G	NP_001128496.1:p.Pro251Arg
NM_001166158.1:c.343-17775C>G	NP_001159630.1:n.343-17775C>G
NM_003477.2:c.797C>G	NP_003468.2:p.Pro266Arg
XM_011520390.1:c.617C>G	XP_011518692.1:p.Pro206Arg
NM_003477.3:c.797C>G MANE Select	NP_003468.2:p.Pro266Arg
NM_001135024.2:c.617C>G	NP_001128496.2:p.Pro206Arg
NM_001166158.2:c.343-17775C>G	NP_001159630.1:n.343-17775C>G