Canonical Allele Identifier: CA2262900633

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946670G= , CM000679.2:g.47946670G=	GRCh38
NC_000017.10:g.46024036G= , CM000679.1:g.46024036G=	GRCh37
NC_000017.9:g.43379035G=	NCBI36
NG_008744.1:g.10148G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018129.4:c.674G= MANE Select	NP_060599.1:p.Arg225=
ENST00000642017.2:c.674G= MANE Select	ENSP00000493302.2:p.Arg225=
NM_018129.3:c.674G=	NP_060599.1:p.Arg225=
ENST00000225573.4:c.674G=	ENSP00000225573.4:p.Arg225=
ENST00000225573.5:c.545G=	ENSP00000225573.5:p.Arg182=
ENST00000434554.6:c.545G=	ENSP00000399960.2:p.Arg182=
ENST00000434554.7:c.620G=	ENSP00000399960.3:p.Arg207=
ENST00000582171.5:c.*339G=	ENSP00000463994.1:n.*339G=
ENST00000582171.6:c.*339G=	ENSP00000463994.1:n.*339G=
ENST00000583599.6:c.434G=	ENSP00000463919.2:p.Arg145=
ENST00000584061.6:c.605G=	ENSP00000463972.2:p.Arg202=
ENST00000584806.1:n.343G=
ENST00000584806.2:n.343G=
ENST00000585320.5:c.*156G=	ENSP00000462345.1:n.*156G=
ENST00000641285.1:n.454G=
ENST00000641305.1:n.2173G=
ENST00000641323.1:c.*693G=	ENSP00000492965.1:n.*693G=
ENST00000641427.1:n.674G=
ENST00000641511.1:c.406G=
ENST00000641703.1:c.390G=	ENSP00000493219.1:n.390G=
ENST00000641709.1:c.*496G=	ENSP00000493349.1:n.*496G=
ENST00000641856.1:c.*1182G=	ENSP00000493224.1:n.*1182G=
XM_005257500.2:c.434G=	XP_005257557.1:p.Arg145=
XM_005257500.3:c.434G=	XP_005257557.1:p.Arg145=
XM_011524968.1:c.389G=	XP_011523270.1:p.Arg130=
XM_011524968.2:c.389G=	XP_011523270.1:p.Arg130=
XM_017024813.1:c.434G=	XP_016880302.1:p.Arg145=