Canonical Allele Identifier: CA1963511798

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34978056A= , CM000673.2:g.34978056A=	GRCh38
NC_000011.9:g.34999603A= , CM000673.1:g.34999603A=	GRCh37
NC_000011.8:g.34956179A=	NCBI36
NG_013368.1:g.66927A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000448838.8:c.785-68A=	ENSP00000389404.3:n.785-68A=
ENST00000227868.9:c.965-68A= MANE Select	ENSP00000227868.4:n.965-68A=
ENST00000227868.8:c.965-68A=	ENSP00000227868.4:n.965-68A=
ENST00000430469.6:c.343-6514A=	ENSP00000415695.2:n.343-6514A=
ENST00000448838.7:c.920-68A=	ENSP00000389404.2:n.920-68A=
ENST00000526309.1:c.28-68A=
ENST00000532159.1:n.122A=
NM_001135024.1:c.920-68A=	NP_001128496.1:n.920-68A=
NM_001166158.1:c.343-6514A=	NP_001159630.1:n.343-6514A=
NM_003477.2:c.965-68A=	NP_003468.2:n.965-68A=
XM_011520390.1:c.785-68A=	XP_011518692.1:n.785-68A=
NM_003477.3:c.965-68A= MANE Select	NP_003468.2:n.965-68A=
NM_001135024.2:c.785-68A=	NP_001128496.2:n.785-68A=
NM_001166158.2:c.343-6514A=	NP_001159630.1:n.343-6514A=