Canonical Allele Identifier: CA2262900292

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47945558G= , CM000679.2:g.47945558G=	GRCh38
NC_000017.10:g.46022924G= , CM000679.1:g.46022924G=	GRCh37
NC_000017.9:g.43377923G=	NCBI36
NG_008744.1:g.9036G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018129.4:c.364-1G= MANE Select	NP_060599.1:n.364-1G=
ENST00000642017.2:c.364-1G= MANE Select	ENSP00000493302.2:n.364-1G=
NM_018129.3:c.364-1G=	NP_060599.1:n.364-1G=
ENST00000225573.4:c.364-1G=	ENSP00000225573.4:n.364-1G=
ENST00000225573.5:c.364-1G=	ENSP00000225573.5:n.364-1G=
ENST00000434554.6:c.364-1G=	ENSP00000399960.2:n.364-1G=
ENST00000434554.7:c.364-303G=	ENSP00000399960.3:n.364-303G=
ENST00000582171.5:c.*29-1G=	ENSP00000463994.1:n.*29-1G=
ENST00000582171.6:c.*29-1G=	ENSP00000463994.1:n.*29-1G=
ENST00000583245.5:c.*383-1G=	ENSP00000463520.1:n.*383-1G=
ENST00000583245.6:n.332-1G=
ENST00000583599.5:c.124-1G=	ENSP00000463919.1:n.124-1G=
ENST00000583599.6:c.124-1G=	ENSP00000463919.2:n.124-1G=
ENST00000584061.5:c.*186-1G=	ENSP00000463972.1:n.*186-1G=
ENST00000584061.6:c.334-40G=	ENSP00000463972.2:n.334-40G=
ENST00000584806.1:n.161G=
ENST00000584806.2:n.161G=
ENST00000585320.5:c.*29-765G=	ENSP00000462345.1:n.*29-765G=
ENST00000641285.1:n.144-1G=
ENST00000641305.1:n.1281G=
ENST00000641323.1:c.*383-1G=	ENSP00000492965.1:n.*383-1G=
ENST00000641427.1:n.364-1G=
ENST00000641511.1:c.279-765G=
ENST00000641703.1:c.134-303G=	ENSP00000493219.1:n.134-303G=
ENST00000641709.1:c.*186-1G=	ENSP00000493349.1:n.*186-1G=
ENST00000641856.1:c.*871G=	ENSP00000493224.1:n.*871G=
XM_005257500.2:c.124-1G=	XP_005257557.1:n.124-1G=
XM_005257500.3:c.124-1G=	XP_005257557.1:n.124-1G=
XM_011524968.1:c.79-1G=	XP_011523270.1:n.79-1G=
XM_011524968.2:c.79-1G=	XP_011523270.1:n.79-1G=
XM_017024813.1:c.124-1G=	XP_016880302.1:n.124-1G=