Canonical Allele Identifier: CA2262900660

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946726G= , CM000679.2:g.47946726G=	GRCh38
NC_000017.10:g.46024092G= , CM000679.1:g.46024092G=	GRCh37
NC_000017.9:g.43379091G=	NCBI36
NG_008744.1:g.10204G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225573.5:c.601G=	ENSP00000225573.5:p.Gly201=
ENST00000434554.7:c.676G=	ENSP00000399960.3:p.Gly226=
ENST00000582171.6:c.*395G=	ENSP00000463994.1:n.*395G=
ENST00000583599.6:c.490G=	ENSP00000463919.2:p.Gly164=
ENST00000584061.6:c.661G=	ENSP00000463972.2:p.Gly221=
ENST00000584806.2:n.399G=
ENST00000641305.1:n.2229G=
ENST00000641323.1:c.*749G=	ENSP00000492965.1:n.*749G=
ENST00000641427.1:n.730G=
ENST00000641703.1:c.446G=	ENSP00000493219.1:n.446G=
ENST00000641709.1:c.*552G=	ENSP00000493349.1:n.*552G=
ENST00000641856.1:c.*1238G=	ENSP00000493224.1:n.*1238G=
ENST00000642017.2:c.730G= MANE Select	ENSP00000493302.2:p.Gly244=
ENST00000225573.4:c.730G=	ENSP00000225573.4:p.Gly244=
ENST00000434554.6:c.601G=	ENSP00000399960.2:p.Gly201=
ENST00000582171.5:c.*395G=	ENSP00000463994.1:n.*395G=
ENST00000584806.1:n.399G=
ENST00000585320.5:c.*212G=	ENSP00000462345.1:n.*212G=
NM_018129.3:c.730G=	NP_060599.1:p.Gly244=
XM_005257500.2:c.490G=	XP_005257557.1:p.Gly164=
XM_011524968.1:c.445G=	XP_011523270.1:p.Gly149=
XM_005257500.3:c.490G=	XP_005257557.1:p.Gly164=
XM_011524968.2:c.445G=	XP_011523270.1:p.Gly149=
XM_017024813.1:c.490G=	XP_016880302.1:p.Gly164=
NM_018129.4:c.730G= MANE Select	NP_060599.1:p.Gly244=