Canonical Allele Identifier: CA2262900662

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946729C= , CM000679.2:g.47946729C=	GRCh38
NC_000017.10:g.46024095C= , CM000679.1:g.46024095C=	GRCh37
NC_000017.9:g.43379094C=	NCBI36
NG_008744.1:g.10207C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225573.5:c.604C=	ENSP00000225573.5:p.Pro202=
ENST00000434554.7:c.679C=	ENSP00000399960.3:p.Pro227=
ENST00000582171.6:c.*398C=	ENSP00000463994.1:n.*398C=
ENST00000583599.6:c.493C=	ENSP00000463919.2:p.Pro165=
ENST00000584061.6:c.664C=	ENSP00000463972.2:p.Pro222=
ENST00000584806.2:n.402C=
ENST00000641305.1:n.2232C=
ENST00000641323.1:c.*752C=	ENSP00000492965.1:n.*752C=
ENST00000641427.1:n.733C=
ENST00000641703.1:c.449C=	ENSP00000493219.1:n.449C=
ENST00000641709.1:c.*555C=	ENSP00000493349.1:n.*555C=
ENST00000641856.1:c.*1241C=	ENSP00000493224.1:n.*1241C=
ENST00000642017.2:c.733C= MANE Select	ENSP00000493302.2:p.Pro245=
ENST00000225573.4:c.733C=	ENSP00000225573.4:p.Pro245=
ENST00000434554.6:c.604C=	ENSP00000399960.2:p.Pro202=
ENST00000582171.5:c.*398C=	ENSP00000463994.1:n.*398C=
ENST00000584806.1:n.402C=
ENST00000585320.5:c.*215C=	ENSP00000462345.1:n.*215C=
NM_018129.3:c.733C=	NP_060599.1:p.Pro245=
XM_005257500.2:c.493C=	XP_005257557.1:p.Pro165=
XM_011524968.1:c.448C=	XP_011523270.1:p.Pro150=
XM_005257500.3:c.493C=	XP_005257557.1:p.Pro165=
XM_011524968.2:c.448C=	XP_011523270.1:p.Pro150=
XM_017024813.1:c.493C=	XP_016880302.1:p.Pro165=
NM_018129.4:c.733C= MANE Select	NP_060599.1:p.Pro245=