Canonical Allele Identifier: CA1963422148

Gene: PDHX APIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916482G= , CM000673.2:g.34916482G=	GRCh38
NC_000011.9:g.34938029G= , CM000673.1:g.34938029G=	GRCh37
NC_000011.8:g.34894605G=	NCBI36
NG_013368.1:g.5353G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-25G= (PDHX)	ENSP00000389404.3:n.-25G=
ENST00000395787.3:c.-198C= (APIP)	ENSP00000379133.3:n.-198C=
ENST00000448838.7:c.111G= (PDHX)	ENSP00000389404.2:p.Pro37=
ENST00000533550.5:c.-21+544G= (PDHX)	ENSP00000431281.1:n.-21+544G=
NM_001135024.1:c.111G= (PDHX)	NP_001128496.1:p.Pro37=
NM_001166158.1:c.-174G= (PDHX)	NP_001159630.1:n.-174G=
NM_003477.2:c.-174G= (PDHX)	NP_003468.2:n.-174G=
XM_011520390.1:c.-21+544G= (PDHX)	XP_011518692.1:n.-21+544G=
NM_001135024.2:c.-25G= (PDHX)	NP_001128496.2:n.-25G=