Canonical Allele Identifier: CA1825861332
Gene: NAPRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143575232G= , CM000670.2:g.143575232G= GRCh38
NC_000008.10:g.144657402G= , CM000670.1:g.144657402G= GRCh37
NC_000008.9:g.144728545G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000449291.7:c.1405C= MANE Select ENSP00000401508.2:p.Gln469=
ENST00000340490.7:c.1405C= ENSP00000341136.3:p.Gln469=
ENST00000426292.7:c.1405C= ENSP00000390949.3:p.Gln469=
ENST00000435154.7:c.1405C= ENSP00000405670.3:p.Gln469=
ENST00000449291.6:c.1405C= ENSP00000401508.2:p.Gln469=
ENST00000460623.5:c.383C=
ENST00000464332.5:n.949C=
ENST00000498076.5:n.184C=
ENST00000529179.1:n.92C=
NM_001286829.1:c.1405C= NP_001273758.1:p.Gln469=
NM_145201.5:c.1405C= NP_660202.3:p.Gln469=
XM_011517377.1:c.1291+191C= XP_011515679.1:n.1291+191C=
NM_001363145.1:c.1324C= NP_001350074.1:p.Gln442=
NM_001363146.1:c.721C= NP_001350075.1:p.Gln241=
XM_017013975.2:c.1624C= XP_016869464.1:p.Gln542=
XM_017013976.2:c.1624C= XP_016869465.1:p.Gln542=
XM_017013977.2:c.1324C= XP_016869466.1:p.Gln442=
XM_017013978.2:c.1510+191C= XP_016869467.1:n.1510+191C=
XM_017013979.2:c.721C= XP_016869468.1:p.Gln241=
XM_024447332.1:c.928+191C= XP_024303100.1:n.928+191C=
XM_024447333.1:c.640C= XP_024303101.1:p.Gln214=
NM_145201.6:c.1405C= MANE Select NP_660202.3:p.Gln469=
NM_001286829.2:c.1405C= NP_001273758.1:p.Gln469=