Canonical Allele Identifier: CA1825861364

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575291C= , CM000670.2:g.143575291C=	GRCh38
NC_000008.10:g.144657461C= , CM000670.1:g.144657461C=	GRCh37
NC_000008.9:g.144728604C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1346G= MANE Select	ENSP00000401508.2:p.Gly449=
ENST00000340490.7:c.1346G=	ENSP00000341136.3:p.Gly449=
ENST00000426292.7:c.1346G=	ENSP00000390949.3:p.Gly449=
ENST00000435154.7:c.1346G=	ENSP00000405670.3:p.Gly449=
ENST00000449291.6:c.1346G=	ENSP00000401508.2:p.Gly449=
ENST00000460623.5:c.324G=
ENST00000464332.5:n.890G=
ENST00000498076.5:n.125G=
ENST00000529179.1:n.33G=
NM_001286829.1:c.1346G=	NP_001273758.1:p.Gly449=
NM_145201.5:c.1346G=	NP_660202.3:p.Gly449=
XM_011517377.1:c.1291+132G=	XP_011515679.1:n.1291+132G=
NM_001363145.1:c.1265G=	NP_001350074.1:p.Gly422=
NM_001363146.1:c.662G=	NP_001350075.1:p.Gly221=
XM_017013975.2:c.1565G=	XP_016869464.1:p.Gly522=
XM_017013976.2:c.1565G=	XP_016869465.1:p.Gly522=
XM_017013977.2:c.1265G=	XP_016869466.1:p.Gly422=
XM_017013978.2:c.1510+132G=	XP_016869467.1:n.1510+132G=
XM_017013979.2:c.662G=	XP_016869468.1:p.Gly221=
XM_024447332.1:c.928+132G=	XP_024303100.1:n.928+132G=
XM_024447333.1:c.581G=	XP_024303101.1:p.Gly194=
NM_145201.6:c.1346G= MANE Select	NP_660202.3:p.Gly449=
NM_001286829.2:c.1346G=	NP_001273758.1:p.Gly449=