Canonical Allele Identifier: CA1963497565

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34994922A= , CM000673.2:g.34994922A=	GRCh38
NC_000011.9:g.35016469A= , CM000673.1:g.35016469A=	GRCh37
NC_000011.8:g.34973045A=	NCBI36
NG_013368.1:g.83793A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003477.3:c.1256A= MANE Select	NP_003468.2:p.Asn419=
ENST00000227868.9:c.1256A= MANE Select	ENSP00000227868.4:p.Asn419=
NM_001135024.1:c.1211A=	NP_001128496.1:p.Asn404=
NM_001135024.2:c.1076A=	NP_001128496.2:p.Asn359=
NM_001166158.1:c.575A=	NP_001159630.1:p.Asn192=
NM_001166158.2:c.575A=	NP_001159630.1:p.Asn192=
NM_003477.2:c.1256A=	NP_003468.2:p.Asn419=
ENST00000227868.8:c.1256A=	ENSP00000227868.4:p.Asn419=
ENST00000430469.6:c.575A=	ENSP00000415695.2:p.Asn192=
ENST00000448838.7:c.1211A=	ENSP00000389404.2:p.Asn404=
ENST00000448838.8:c.1076A=	ENSP00000389404.3:p.Asn359=
ENST00000477173.3:n.161+2543A=
ENST00000526309.1:c.319A=
XM_011520390.1:c.1076A=	XP_011518692.1:p.Asn359=