Canonical Allele Identifier: CA2262900689

Gene: PNPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47946780T= , CM000679.2:g.47946780T=	GRCh38
NC_000017.10:g.46024146T= , CM000679.1:g.46024146T=	GRCh37
NC_000017.9:g.43379145T=	NCBI36
NG_008744.1:g.10258T=

Transcript Alleles

HGVS	Amino-acid Change
NM_018129.4:c.784T= MANE Select	NP_060599.1:p.Ter262=
ENST00000642017.2:c.784T= MANE Select	ENSP00000493302.2:p.Ter262=
NM_018129.3:c.784T=	NP_060599.1:p.Ter262=
ENST00000225573.4:c.784T=	ENSP00000225573.4:p.Ter262=
ENST00000225573.5:c.655T=	ENSP00000225573.5:p.Ter219=
ENST00000434554.6:c.655T=	ENSP00000399960.2:p.Ter219=
ENST00000434554.7:c.730T=	ENSP00000399960.3:p.Ter244=
ENST00000582171.5:c.*449T=	ENSP00000463994.1:n.*449T=
ENST00000582171.6:c.*449T=	ENSP00000463994.1:n.*449T=
ENST00000584061.6:c.715T=	ENSP00000463972.2:p.Ter239=
ENST00000584806.1:n.453T=
ENST00000584806.2:n.453T=
ENST00000641305.1:n.2283T=
ENST00000641323.1:c.*803T=	ENSP00000492965.1:n.*803T=
ENST00000641427.1:n.784T=
ENST00000641703.1:c.500T=	ENSP00000493219.1:n.500T=
ENST00000641709.1:c.*606T=	ENSP00000493349.1:n.*606T=
ENST00000641856.1:c.*1292T=	ENSP00000493224.1:n.*1292T=
XM_005257500.2:c.544T=	XP_005257557.1:p.Ter182=
XM_005257500.3:c.544T=	XP_005257557.1:p.Ter182=
XM_011524968.1:c.499T=	XP_011523270.1:p.Ter167=
XM_011524968.2:c.499T=	XP_011523270.1:p.Ter167=
XM_017024813.1:c.544T=	XP_016880302.1:p.Ter182=