Canonical Allele Identifier: CA1825861464
Gene: NAPRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143575455C= , CM000670.2:g.143575455C= GRCh38
NC_000008.10:g.144657625C= , CM000670.1:g.144657625C= GRCh37
NC_000008.9:g.144728768C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000449291.7:c.1259G= MANE Select ENSP00000401508.2:p.Ser420=
ENST00000340490.7:c.1259G= ENSP00000341136.3:p.Ser420=
ENST00000426292.7:c.1259G= ENSP00000390949.3:p.Ser420=
ENST00000435154.7:c.1259G= ENSP00000405670.3:p.Ser420=
ENST00000449291.6:c.1259G= ENSP00000401508.2:p.Ser420=
ENST00000460623.5:c.237G=
ENST00000464332.5:n.803G=
ENST00000525583.5:c.1043G=
NM_001286829.1:c.1259G= NP_001273758.1:p.Ser420=
NM_145201.5:c.1259G= NP_660202.3:p.Ser420=
XM_011517377.1:c.1259G= XP_011515679.1:p.Ser420=
NM_001363145.1:c.1178G= NP_001350074.1:p.Ser393=
NM_001363146.1:c.575G= NP_001350075.1:p.Ser192=
XM_017013975.2:c.1478G= XP_016869464.1:p.Ser493=
XM_017013976.2:c.1478G= XP_016869465.1:p.Ser493=
XM_017013977.2:c.1178G= XP_016869466.1:p.Ser393=
XM_017013978.2:c.1478G= XP_016869467.1:p.Ser493=
XM_017013979.2:c.575G= XP_016869468.1:p.Ser192=
XM_024447332.1:c.896G= XP_024303100.1:p.Ser299=
XM_024447333.1:c.494G= XP_024303101.1:p.Ser165=
NM_145201.6:c.1259G= MANE Select NP_660202.3:p.Ser420=
NM_001286829.2:c.1259G= NP_001273758.1:p.Ser420=