Canonical Allele Identifier: CA2262900653

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946714G= , CM000679.2:g.47946714G=	GRCh38
NC_000017.10:g.46024080G= , CM000679.1:g.46024080G=	GRCh37
NC_000017.9:g.43379079G=	NCBI36
NG_008744.1:g.10192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.589G=	ENSP00000225573.5:p.Asp197=
ENST00000434554.7:c.664G=	ENSP00000399960.3:p.Asp222=
ENST00000582171.6:c.*383G=	ENSP00000463994.1:n.*383G=
ENST00000583599.6:c.478G=	ENSP00000463919.2:p.Asp160=
ENST00000584061.6:c.649G=	ENSP00000463972.2:p.Asp217=
ENST00000584806.2:n.387G=
ENST00000641305.1:n.2217G=
ENST00000641323.1:c.*737G=	ENSP00000492965.1:n.*737G=
ENST00000641427.1:n.718G=
ENST00000641511.1:c.450G=
ENST00000641703.1:c.434G=	ENSP00000493219.1:n.434G=
ENST00000641709.1:c.*540G=	ENSP00000493349.1:n.*540G=
ENST00000641856.1:c.*1226G=	ENSP00000493224.1:n.*1226G=
ENST00000642017.2:c.718G= MANE Select	ENSP00000493302.2:p.Asp240=
ENST00000225573.4:c.718G=	ENSP00000225573.4:p.Asp240=
ENST00000434554.6:c.589G=	ENSP00000399960.2:p.Asp197=
ENST00000582171.5:c.*383G=	ENSP00000463994.1:n.*383G=
ENST00000584806.1:n.387G=
ENST00000585320.5:c.*200G=	ENSP00000462345.1:n.*200G=
NM_018129.3:c.718G=	NP_060599.1:p.Asp240=
XM_005257500.2:c.478G=	XP_005257557.1:p.Asp160=
XM_011524968.1:c.433G=	XP_011523270.1:p.Asp145=
XM_005257500.3:c.478G=	XP_005257557.1:p.Asp160=
XM_011524968.2:c.433G=	XP_011523270.1:p.Asp145=
XM_017024813.1:c.478G=	XP_016880302.1:p.Asp160=
NM_018129.4:c.718G= MANE Select	NP_060599.1:p.Asp240=