Canonical Allele Identifier: CA2262900610

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946622A= , CM000679.2:g.47946622A=	GRCh38
NC_000017.10:g.46023988A= , CM000679.1:g.46023988A=	GRCh37
NC_000017.9:g.43378987A=	NCBI36
NG_008744.1:g.10100A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.497A=	ENSP00000225573.5:p.Tyr166=
ENST00000434554.7:c.572A=	ENSP00000399960.3:p.Tyr191=
ENST00000582171.6:c.*291A=	ENSP00000463994.1:n.*291A=
ENST00000583599.6:c.386A=	ENSP00000463919.2:p.Tyr129=
ENST00000584061.6:c.557A=	ENSP00000463972.2:p.Tyr186=
ENST00000584806.2:n.295A=
ENST00000641285.1:n.406A=
ENST00000641305.1:n.2125A=
ENST00000641323.1:c.*645A=	ENSP00000492965.1:n.*645A=
ENST00000641427.1:n.626A=
ENST00000641511.1:c.358A=
ENST00000641703.1:c.342A=	ENSP00000493219.1:n.342A=
ENST00000641709.1:c.*448A=	ENSP00000493349.1:n.*448A=
ENST00000641856.1:c.*1134A=	ENSP00000493224.1:n.*1134A=
ENST00000642017.2:c.626A= MANE Select	ENSP00000493302.2:p.Tyr209=
ENST00000225573.4:c.626A=	ENSP00000225573.4:p.Tyr209=
ENST00000434554.6:c.497A=	ENSP00000399960.2:p.Tyr166=
ENST00000582171.5:c.*291A=	ENSP00000463994.1:n.*291A=
ENST00000584806.1:n.295A=
ENST00000585320.5:c.*108A=	ENSP00000462345.1:n.*108A=
NM_018129.3:c.626A=	NP_060599.1:p.Tyr209=
XM_005257500.2:c.386A=	XP_005257557.1:p.Tyr129=
XM_011524968.1:c.341A=	XP_011523270.1:p.Tyr114=
XM_005257500.3:c.386A=	XP_005257557.1:p.Tyr129=
XM_011524968.2:c.341A=	XP_011523270.1:p.Tyr114=
XM_017024813.1:c.386A=	XP_016880302.1:p.Tyr129=
NM_018129.4:c.626A= MANE Select	NP_060599.1:p.Tyr209=