Canonical Allele Identifier: CA1963495450

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34992363C= , CM000673.2:g.34992363C=	GRCh38
NC_000011.9:g.35013910C= , CM000673.1:g.35013910C=	GRCh37
NC_000011.8:g.34970486C=	NCBI36
NG_013368.1:g.81234C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003477.3:c.1231C= MANE Select	NP_003468.2:p.Gln411=
ENST00000227868.9:c.1231C= MANE Select	ENSP00000227868.4:p.Gln411=
NM_001135024.1:c.1186C=	NP_001128496.1:p.Gln396=
NM_001135024.2:c.1051C=	NP_001128496.2:p.Gln351=
NM_001166158.1:c.550C=	NP_001159630.1:p.Gln184=
NM_001166158.2:c.550C=	NP_001159630.1:p.Gln184=
NM_003477.2:c.1231C=	NP_003468.2:p.Gln411=
ENST00000227868.8:c.1231C=	ENSP00000227868.4:p.Gln411=
ENST00000430469.6:c.550C=	ENSP00000415695.2:p.Gln184=
ENST00000448838.7:c.1186C=	ENSP00000389404.2:p.Gln396=
ENST00000448838.8:c.1051C=	ENSP00000389404.3:p.Gln351=
ENST00000477173.3:n.145C=
ENST00000526309.1:c.294C=
XM_011520390.1:c.1051C=	XP_011518692.1:p.Gln351=