Canonical Allele Identifier: CA2739973658

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574939G>T , CM000670.2:g.143574939G>T	GRCh38
NC_000008.10:g.144657109G>T , CM000670.1:g.144657109G>T	GRCh37
NC_000008.9:g.144728252G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1555-39C>A MANE Select	ENSP00000401508.2:n.1555-39C>A
ENST00000340490.7:c.1601C>A	ENSP00000341136.3:p.Pro534His
ENST00000426292.7:c.1516-39C>A	ENSP00000390949.3:n.1516-39C>A
ENST00000435154.7:c.*225C>A	ENSP00000405670.3:n.*225C>A
ENST00000449291.6:c.1555-39C>A	ENSP00000401508.2:n.1555-39C>A
ENST00000460623.5:c.540C>A
ENST00000464332.5:n.1099-39C>A
ENST00000498076.5:n.334-39C>A
ENST00000529179.1:n.339-39C>A
NM_001286829.1:c.1516-39C>A	NP_001273758.1:n.1516-39C>A
NM_145201.5:c.1555-39C>A	NP_660202.3:n.1555-39C>A
XM_011517377.1:c.1292-39C>A	XP_011515679.1:n.1292-39C>A
NM_001363145.1:c.1474-39C>A	NP_001350074.1:n.1474-39C>A
NM_001363146.1:c.871-39C>A	NP_001350075.1:n.871-39C>A
XM_017013975.2:c.1820C>A	XP_016869464.1:p.Pro607His
XM_017013976.2:c.1774-39C>A	XP_016869465.1:n.1774-39C>A
XM_017013977.2:c.1520C>A	XP_016869466.1:p.Pro507His
XM_017013978.2:c.1511-39C>A	XP_016869467.1:n.1511-39C>A
XM_017013979.2:c.917C>A	XP_016869468.1:p.Pro306His
XM_024447332.1:c.929-39C>A	XP_024303100.1:n.929-39C>A
XM_024447333.1:c.836C>A	XP_024303101.1:p.Pro279His
NM_145201.6:c.1555-39C>A MANE Select	NP_660202.3:n.1555-39C>A
NM_001286829.2:c.1516-39C>A	NP_001273758.1:n.1516-39C>A