Canonical Allele Identifier: CA1963422569

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916699G= , CM000673.2:g.34916699G=	GRCh38
NC_000011.9:g.34938246G= , CM000673.1:g.34938246G=	GRCh37
NC_000011.8:g.34894822G=	NCBI36
NG_013368.1:g.5570G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003477.3:c.44G= MANE Select	NP_003468.2:p.Arg15=
ENST00000227868.9:c.44G= MANE Select	ENSP00000227868.4:p.Arg15=
NM_001135024.1:c.115+213G=	NP_001128496.1:n.115+213G=
NM_001135024.2:c.-21+213G=	NP_001128496.2:n.-21+213G=
NM_001166158.1:c.44G=	NP_001159630.1:p.Arg15=
NM_001166158.2:c.44G=	NP_001159630.1:p.Arg15=
NM_003477.2:c.44G=	NP_003468.2:p.Arg15=
ENST00000227868.8:c.44G=	ENSP00000227868.4:p.Arg15=
ENST00000430469.6:c.44G=	ENSP00000415695.2:p.Arg15=
ENST00000448838.7:c.115+213G=	ENSP00000389404.2:n.115+213G=
ENST00000448838.8:c.-21+213G=	ENSP00000389404.3:n.-21+213G=
ENST00000533262.1:c.44G=	ENSP00000432277.1:p.Arg15=
ENST00000533550.5:c.-21+761G=	ENSP00000431281.1:n.-21+761G=
XM_011520390.1:c.-21+761G=	XP_011518692.1:n.-21+761G=