Canonical Allele Identifier: CA2580840268

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574953A>C , CM000670.2:g.143574953A>C	GRCh38
NC_000008.10:g.144657123A>C , CM000670.1:g.144657123A>C	GRCh37
NC_000008.9:g.144728266A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1554+33T>G MANE Select	ENSP00000401508.2:n.1554+33T>G
ENST00000340490.7:c.1587T>G	ENSP00000341136.3:p.Pro529=
ENST00000426292.7:c.1515+33T>G	ENSP00000390949.3:n.1515+33T>G
ENST00000435154.7:c.*211T>G	ENSP00000405670.3:n.*211T>G
ENST00000449291.6:c.1554+33T>G	ENSP00000401508.2:n.1554+33T>G
ENST00000460623.5:c.526T>G
ENST00000464332.5:n.1098+33T>G
ENST00000498076.5:n.333+33T>G
ENST00000529179.1:n.338+33T>G
NM_001286829.1:c.1515+33T>G	NP_001273758.1:n.1515+33T>G
NM_145201.5:c.1554+33T>G	NP_660202.3:n.1554+33T>G
XM_011517377.1:c.1292-53T>G	XP_011515679.1:n.1292-53T>G
NM_001363145.1:c.1473+33T>G	NP_001350074.1:n.1473+33T>G
NM_001363146.1:c.870+33T>G	NP_001350075.1:n.870+33T>G
XM_017013975.2:c.1806T>G	XP_016869464.1:p.Pro602=
XM_017013976.2:c.1773+33T>G	XP_016869465.1:n.1773+33T>G
XM_017013977.2:c.1506T>G	XP_016869466.1:p.Pro502=
XM_017013978.2:c.1511-53T>G	XP_016869467.1:n.1511-53T>G
XM_017013979.2:c.903T>G	XP_016869468.1:p.Pro301=
XM_024447332.1:c.929-53T>G	XP_024303100.1:n.929-53T>G
XM_024447333.1:c.822T>G	XP_024303101.1:p.Pro274=
NM_145201.6:c.1554+33T>G MANE Select	NP_660202.3:n.1554+33T>G
NM_001286829.2:c.1515+33T>G	NP_001273758.1:n.1515+33T>G