Canonical Allele Identifier: CA1825861171

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574971G= , CM000670.2:g.143574971G=	GRCh38
NC_000008.10:g.144657141G= , CM000670.1:g.144657141G=	GRCh37
NC_000008.9:g.144728284G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1554+15C= MANE Select	ENSP00000401508.2:n.1554+15C=
ENST00000340490.7:c.1569C=	ENSP00000341136.3:p.Pro523=
ENST00000426292.7:c.1515+15C=	ENSP00000390949.3:n.1515+15C=
ENST00000435154.7:c.*193C=	ENSP00000405670.3:n.*193C=
ENST00000449291.6:c.1554+15C=	ENSP00000401508.2:n.1554+15C=
ENST00000460623.5:c.508C=
ENST00000464332.5:n.1098+15C=
ENST00000498076.5:n.333+15C=
ENST00000529179.1:n.338+15C=
NM_001286829.1:c.1515+15C=	NP_001273758.1:n.1515+15C=
NM_145201.5:c.1554+15C=	NP_660202.3:n.1554+15C=
XM_011517377.1:c.1292-71C=	XP_011515679.1:n.1292-71C=
NM_001363145.1:c.1473+15C=	NP_001350074.1:n.1473+15C=
NM_001363146.1:c.870+15C=	NP_001350075.1:n.870+15C=
XM_017013975.2:c.1788C=	XP_016869464.1:p.Pro596=
XM_017013976.2:c.1773+15C=	XP_016869465.1:n.1773+15C=
XM_017013977.2:c.1488C=	XP_016869466.1:p.Pro496=
XM_017013978.2:c.1511-71C=	XP_016869467.1:n.1511-71C=
XM_017013979.2:c.885C=	XP_016869468.1:p.Pro295=
XM_024447332.1:c.929-71C=	XP_024303100.1:n.929-71C=
XM_024447333.1:c.804C=	XP_024303101.1:p.Pro268=
NM_145201.6:c.1554+15C= MANE Select	NP_660202.3:n.1554+15C=
NM_001286829.2:c.1515+15C=	NP_001273758.1:n.1515+15C=