Canonical Allele Identifier: CA2262900592

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946584G= , CM000679.2:g.47946584G=	GRCh38
NC_000017.10:g.46023950G= , CM000679.1:g.46023950G=	GRCh37
NC_000017.9:g.43378949G=	NCBI36
NG_008744.1:g.10062G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.489-30G=	ENSP00000225573.5:n.489-30G=
ENST00000434554.7:c.564-30G=	ENSP00000399960.3:n.564-30G=
ENST00000582171.6:c.*283-30G=	ENSP00000463994.1:n.*283-30G=
ENST00000583599.6:c.378-30G=	ENSP00000463919.2:n.378-30G=
ENST00000584061.6:c.549-30G=	ENSP00000463972.2:n.549-30G=
ENST00000584806.2:n.287-30G=
ENST00000641285.1:n.398-30G=
ENST00000641305.1:n.2117-30G=
ENST00000641323.1:c.*637-30G=	ENSP00000492965.1:n.*637-30G=
ENST00000641427.1:n.618-30G=
ENST00000641511.1:c.350-30G=
ENST00000641703.1:c.334-30G=	ENSP00000493219.1:n.334-30G=
ENST00000641709.1:c.*440-30G=	ENSP00000493349.1:n.*440-30G=
ENST00000641856.1:c.*1126-30G=	ENSP00000493224.1:n.*1126-30G=
ENST00000642017.2:c.618-30G= MANE Select	ENSP00000493302.2:n.618-30G=
ENST00000225573.4:c.618-30G=	ENSP00000225573.4:n.618-30G=
ENST00000434554.6:c.489-30G=	ENSP00000399960.2:n.489-30G=
ENST00000582171.5:c.*283-30G=	ENSP00000463994.1:n.*283-30G=
ENST00000584806.1:n.287-30G=
ENST00000585320.5:c.*100-30G=	ENSP00000462345.1:n.*100-30G=
NM_018129.3:c.618-30G=	NP_060599.1:n.618-30G=
XM_005257500.2:c.378-30G=	XP_005257557.1:n.378-30G=
XM_011524968.1:c.333-30G=	XP_011523270.1:n.333-30G=
XM_005257500.3:c.378-30G=	XP_005257557.1:n.378-30G=
XM_011524968.2:c.333-30G=	XP_011523270.1:n.333-30G=
XM_017024813.1:c.378-30G=	XP_016880302.1:n.378-30G=
NM_018129.4:c.618-30G= MANE Select	NP_060599.1:n.618-30G=