Canonical Allele Identifier: CA1963501760

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34966720C= , CM000673.2:g.34966720C=	GRCh38
NC_000011.9:g.34988267C= , CM000673.1:g.34988267C=	GRCh37
NC_000011.8:g.34944843C=	NCBI36
NG_013368.1:g.55591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.542C=	ENSP00000389404.3:p.Pro181=
ENST00000227868.9:c.722C= MANE Select	ENSP00000227868.4:p.Pro241=
ENST00000227868.8:c.722C=	ENSP00000227868.4:p.Pro241=
ENST00000430469.6:c.343-17850C=	ENSP00000415695.2:n.343-17850C=
ENST00000448838.7:c.677C=	ENSP00000389404.2:p.Pro226=
NM_001135024.1:c.677C=	NP_001128496.1:p.Pro226=
NM_001166158.1:c.343-17850C=	NP_001159630.1:n.343-17850C=
NM_003477.2:c.722C=	NP_003468.2:p.Pro241=
XM_011520390.1:c.542C=	XP_011518692.1:p.Pro181=
NM_003477.3:c.722C= MANE Select	NP_003468.2:p.Pro241=
NM_001135024.2:c.542C=	NP_001128496.2:p.Pro181=
NM_001166158.2:c.343-17850C=	NP_001159630.1:n.343-17850C=