Canonical Allele Identifier: CA2262900764

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946972G= , CM000679.2:g.47946972G=	GRCh38
NC_000017.10:g.46024338G= , CM000679.1:g.46024338G=	GRCh37
NC_000017.9:g.43379337G=	NCBI36
NG_008744.1:g.10450G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.*190G=	ENSP00000225573.5:n.*190G=
ENST00000434554.7:c.*190G=	ENSP00000399960.3:n.*190G=
ENST00000582171.6:c.*641G=	ENSP00000463994.1:n.*641G=
ENST00000584806.2:n.645G=
ENST00000641305.1:n.2475G=
ENST00000641323.1:c.*995G=	ENSP00000492965.1:n.*995G=
ENST00000641427.1:n.976G=
ENST00000641703.1:c.692G=	ENSP00000493219.1:n.692G=
ENST00000641709.1:c.*798G=	ENSP00000493349.1:n.*798G=
ENST00000641856.1:c.*1484G=	ENSP00000493224.1:n.*1484G=
ENST00000642017.2:c.*190G= MANE Select	ENSP00000493302.2:n.*190G=
ENST00000225573.4:c.*190G=	ENSP00000225573.4:n.*190G=
ENST00000434554.6:c.*190G=	ENSP00000399960.2:n.*190G=
ENST00000582171.5:c.*641G=	ENSP00000463994.1:n.*641G=
NM_018129.3:c.*190G=	NP_060599.1:n.*190G=
XM_005257500.2:c.*190G=	XP_005257557.1:n.*190G=
XM_011524968.1:c.*190G=	XP_011523270.1:n.*190G=
XM_005257500.3:c.*190G=	XP_005257557.1:n.*190G=
XM_011524968.2:c.*190G=	XP_011523270.1:n.*190G=
XM_017024813.1:c.*190G=	XP_016880302.1:n.*190G=
NM_018129.4:c.*190G= MANE Select	NP_060599.1:n.*190G=