Canonical Allele Identifier: CA1825861154

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574940G= , CM000670.2:g.143574940G=	GRCh38
NC_000008.10:g.144657110G= , CM000670.1:g.144657110G=	GRCh37
NC_000008.9:g.144728253G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1555-40C= MANE Select	ENSP00000401508.2:n.1555-40C=
ENST00000340490.7:c.1600C=	ENSP00000341136.3:p.Pro534=
ENST00000426292.7:c.1516-40C=	ENSP00000390949.3:n.1516-40C=
ENST00000435154.7:c.*224C=	ENSP00000405670.3:n.*224C=
ENST00000449291.6:c.1555-40C=	ENSP00000401508.2:n.1555-40C=
ENST00000460623.5:c.539C=
ENST00000464332.5:n.1099-40C=
ENST00000498076.5:n.334-40C=
ENST00000529179.1:n.339-40C=
NM_001286829.1:c.1516-40C=	NP_001273758.1:n.1516-40C=
NM_145201.5:c.1555-40C=	NP_660202.3:n.1555-40C=
XM_011517377.1:c.1292-40C=	XP_011515679.1:n.1292-40C=
NM_001363145.1:c.1474-40C=	NP_001350074.1:n.1474-40C=
NM_001363146.1:c.871-40C=	NP_001350075.1:n.871-40C=
XM_017013975.2:c.1819C=	XP_016869464.1:p.Pro607=
XM_017013976.2:c.1774-40C=	XP_016869465.1:n.1774-40C=
XM_017013977.2:c.1519C=	XP_016869466.1:p.Pro507=
XM_017013978.2:c.1511-40C=	XP_016869467.1:n.1511-40C=
XM_017013979.2:c.916C=	XP_016869468.1:p.Pro306=
XM_024447332.1:c.929-40C=	XP_024303100.1:n.929-40C=
XM_024447333.1:c.835C=	XP_024303101.1:p.Pro279=
NM_145201.6:c.1555-40C= MANE Select	NP_660202.3:n.1555-40C=
NM_001286829.2:c.1516-40C=	NP_001273758.1:n.1516-40C=