Canonical Allele Identifier: CA2262900645

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946697G= , CM000679.2:g.47946697G=	GRCh38
NC_000017.10:g.46024063G= , CM000679.1:g.46024063G=	GRCh37
NC_000017.9:g.43379062G=	NCBI36
NG_008744.1:g.10175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225573.5:c.572G=	ENSP00000225573.5:p.Arg191=
ENST00000434554.7:c.647G=	ENSP00000399960.3:p.Arg216=
ENST00000582171.6:c.*366G=	ENSP00000463994.1:n.*366G=
ENST00000583599.6:c.461G=	ENSP00000463919.2:p.Arg154=
ENST00000584061.6:c.632G=	ENSP00000463972.2:p.Arg211=
ENST00000584806.2:n.370G=
ENST00000641285.1:n.481G=
ENST00000641305.1:n.2200G=
ENST00000641323.1:c.*720G=	ENSP00000492965.1:n.*720G=
ENST00000641427.1:n.701G=
ENST00000641511.1:c.433G=
ENST00000641703.1:c.417G=	ENSP00000493219.1:n.417G=
ENST00000641709.1:c.*523G=	ENSP00000493349.1:n.*523G=
ENST00000641856.1:c.*1209G=	ENSP00000493224.1:n.*1209G=
ENST00000642017.2:c.701G= MANE Select	ENSP00000493302.2:p.Arg234=
ENST00000225573.4:c.701G=	ENSP00000225573.4:p.Arg234=
ENST00000434554.6:c.572G=	ENSP00000399960.2:p.Arg191=
ENST00000582171.5:c.*366G=	ENSP00000463994.1:n.*366G=
ENST00000584806.1:n.370G=
ENST00000585320.5:c.*183G=	ENSP00000462345.1:n.*183G=
NM_018129.3:c.701G=	NP_060599.1:p.Arg234=
XM_005257500.2:c.461G=	XP_005257557.1:p.Arg154=
XM_011524968.1:c.416G=	XP_011523270.1:p.Arg139=
XM_005257500.3:c.461G=	XP_005257557.1:p.Arg154=
XM_011524968.2:c.416G=	XP_011523270.1:p.Arg139=
XM_017024813.1:c.461G=	XP_016880302.1:p.Arg154=
NM_018129.4:c.701G= MANE Select	NP_060599.1:p.Arg234=