Canonical Allele Identifier: CA2739973613

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574907G>T , CM000670.2:g.143574907G>T	GRCh38
NC_000008.10:g.144657077G>T , CM000670.1:g.144657077G>T	GRCh37
NC_000008.9:g.144728220G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1555-7C>A MANE Select	ENSP00000401508.2:n.1555-7C>A
ENST00000340490.7:c.1633C>A	ENSP00000341136.3:p.Pro545Thr
ENST00000426292.7:c.1516-7C>A	ENSP00000390949.3:n.1516-7C>A
ENST00000435154.7:c.*257C>A	ENSP00000405670.3:n.*257C>A
ENST00000449291.6:c.1555-7C>A	ENSP00000401508.2:n.1555-7C>A
ENST00000460623.5:c.572C>A
ENST00000464332.5:n.1099-7C>A
ENST00000498076.5:n.334-7C>A
ENST00000529179.1:n.339-7C>A
NM_001286829.1:c.1516-7C>A	NP_001273758.1:n.1516-7C>A
NM_145201.5:c.1555-7C>A	NP_660202.3:n.1555-7C>A
XM_011517377.1:c.1292-7C>A	XP_011515679.1:n.1292-7C>A
NM_001363145.1:c.1474-7C>A	NP_001350074.1:n.1474-7C>A
NM_001363146.1:c.871-7C>A	NP_001350075.1:n.871-7C>A
XM_017013975.2:c.1852C>A	XP_016869464.1:p.Pro618Thr
XM_017013976.2:c.1774-7C>A	XP_016869465.1:n.1774-7C>A
XM_017013977.2:c.1552C>A	XP_016869466.1:p.Pro518Thr
XM_017013978.2:c.1511-7C>A	XP_016869467.1:n.1511-7C>A
XM_017013979.2:c.949C>A	XP_016869468.1:p.Pro317Thr
XM_024447332.1:c.929-7C>A	XP_024303100.1:n.929-7C>A
XM_024447333.1:c.868C>A	XP_024303101.1:p.Pro290Thr
NM_145201.6:c.1555-7C>A MANE Select	NP_660202.3:n.1555-7C>A
NM_001286829.2:c.1516-7C>A	NP_001273758.1:n.1516-7C>A