Canonical Allele Identifier: CA2739973710

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574968G>A , CM000670.2:g.143574968G>A	GRCh38
NC_000008.10:g.144657138G>A , CM000670.1:g.144657138G>A	GRCh37
NC_000008.9:g.144728281G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1554+18C>T MANE Select	ENSP00000401508.2:n.1554+18C>T
ENST00000340490.7:c.1572C>T	ENSP00000341136.3:p.Thr524=
ENST00000426292.7:c.1515+18C>T	ENSP00000390949.3:n.1515+18C>T
ENST00000435154.7:c.*196C>T	ENSP00000405670.3:n.*196C>T
ENST00000449291.6:c.1554+18C>T	ENSP00000401508.2:n.1554+18C>T
ENST00000460623.5:c.511C>T
ENST00000464332.5:n.1098+18C>T
ENST00000498076.5:n.333+18C>T
ENST00000529179.1:n.338+18C>T
NM_001286829.1:c.1515+18C>T	NP_001273758.1:n.1515+18C>T
NM_145201.5:c.1554+18C>T	NP_660202.3:n.1554+18C>T
XM_011517377.1:c.1292-68C>T	XP_011515679.1:n.1292-68C>T
NM_001363145.1:c.1473+18C>T	NP_001350074.1:n.1473+18C>T
NM_001363146.1:c.870+18C>T	NP_001350075.1:n.870+18C>T
XM_017013975.2:c.1791C>T	XP_016869464.1:p.Thr597=
XM_017013976.2:c.1773+18C>T	XP_016869465.1:n.1773+18C>T
XM_017013977.2:c.1491C>T	XP_016869466.1:p.Thr497=
XM_017013978.2:c.1511-68C>T	XP_016869467.1:n.1511-68C>T
XM_017013979.2:c.888C>T	XP_016869468.1:p.Thr296=
XM_024447332.1:c.929-68C>T	XP_024303100.1:n.929-68C>T
XM_024447333.1:c.807C>T	XP_024303101.1:p.Thr269=
NM_145201.6:c.1554+18C>T MANE Select	NP_660202.3:n.1554+18C>T
NM_001286829.2:c.1515+18C>T	NP_001273758.1:n.1515+18C>T