Canonical Allele Identifier: CA1963422651

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916739G= , CM000673.2:g.34916739G=	GRCh38
NC_000011.9:g.34938286G= , CM000673.1:g.34938286G=	GRCh37
NC_000011.8:g.34894862G=	NCBI36
NG_013368.1:g.5610G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-21+253G=	ENSP00000389404.3:n.-21+253G=
ENST00000227868.9:c.84G= MANE Select	ENSP00000227868.4:p.Leu28=
ENST00000227868.8:c.84G=	ENSP00000227868.4:p.Leu28=
ENST00000430469.6:c.84G=	ENSP00000415695.2:p.Leu28=
ENST00000448838.7:c.115+253G=	ENSP00000389404.2:n.115+253G=
ENST00000533262.1:c.84G=	ENSP00000432277.1:p.Leu28=
ENST00000533550.5:c.-21+801G=	ENSP00000431281.1:n.-21+801G=
NM_001135024.1:c.115+253G=	NP_001128496.1:n.115+253G=
NM_001166158.1:c.84G=	NP_001159630.1:p.Leu28=
NM_003477.2:c.84G=	NP_003468.2:p.Leu28=
XM_011520390.1:c.-21+801G=	XP_011518692.1:n.-21+801G=
NM_003477.3:c.84G= MANE Select	NP_003468.2:p.Leu28=
NM_001135024.2:c.-21+253G=	NP_001128496.2:n.-21+253G=
NM_001166158.2:c.84G=	NP_001159630.1:p.Leu28=