Canonical Allele Identifier: CA1825861210

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575032C= , CM000670.2:g.143575032C=	GRCh38
NC_000008.10:g.144657202C= , CM000670.1:g.144657202C=	GRCh37
NC_000008.9:g.144728345C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1508G= MANE Select	ENSP00000401508.2:p.Arg503=
ENST00000340490.7:c.1508G=	ENSP00000341136.3:p.Arg503=
ENST00000426292.7:c.1469G=	ENSP00000390949.3:p.Arg490=
ENST00000435154.7:c.*132G=	ENSP00000405670.3:n.*132G=
ENST00000449291.6:c.1508G=	ENSP00000401508.2:p.Arg503=
ENST00000460623.5:c.447G=
ENST00000464332.5:n.1052G=
ENST00000498076.5:n.287G=
ENST00000529179.1:n.292G=
NM_001286829.1:c.1469G=	NP_001273758.1:p.Arg490=
NM_145201.5:c.1508G=	NP_660202.3:p.Arg503=
XM_011517377.1:c.1292-132G=	XP_011515679.1:n.1292-132G=
NM_001363145.1:c.1427G=	NP_001350074.1:p.Arg476=
NM_001363146.1:c.824G=	NP_001350075.1:p.Arg275=
XM_017013975.2:c.1727G=	XP_016869464.1:p.Arg576=
XM_017013976.2:c.1727G=	XP_016869465.1:p.Arg576=
XM_017013977.2:c.1427G=	XP_016869466.1:p.Arg476=
XM_017013978.2:c.1511-132G=	XP_016869467.1:n.1511-132G=
XM_017013979.2:c.824G=	XP_016869468.1:p.Arg275=
XM_024447332.1:c.929-132G=	XP_024303100.1:n.929-132G=
XM_024447333.1:c.743G=	XP_024303101.1:p.Arg248=
NM_145201.6:c.1508G= MANE Select	NP_660202.3:p.Arg503=
NM_001286829.2:c.1469G=	NP_001273758.1:p.Arg490=