Canonical Allele Identifier: CA372448484

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657033C>T (hg19) ; chr8:g.143574863C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574863C>T , CM000670.2:g.143574863C>T	GRCh38
NC_000008.10:g.144657033C>T , CM000670.1:g.144657033C>T	GRCh37
NC_000008.9:g.144728176C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1592G>A MANE Select	ENSP00000401508.2:p.Ser531Asn
ENST00000340490.7:c.1677G>A	ENSP00000341136.3:p.Gln559=
ENST00000426292.7:c.1553G>A	ENSP00000390949.3:p.Ser518Asn
ENST00000435154.7:c.*301G>A	ENSP00000405670.3:n.*301G>A
ENST00000449291.6:c.1592G>A	ENSP00000401508.2:p.Ser531Asn
ENST00000460623.5:c.616G>A
ENST00000464332.5:n.1136G>A
ENST00000498076.5:n.371G>A
ENST00000529179.1:n.376G>A
NM_001286829.1:c.1553G>A	NP_001273758.1:p.Ser518Asn
NM_145201.5:c.1592G>A	NP_660202.3:p.Ser531Asn
XM_011517377.1:c.1329G>A	XP_011515679.1:p.Gln443=
NM_001363145.1:c.1511G>A	NP_001350074.1:p.Ser504Asn
NM_001363146.1:c.908G>A	NP_001350075.1:p.Ser303Asn
XM_017013975.2:c.1896G>A	XP_016869464.1:p.Gln632=
XM_017013976.2:c.1811G>A	XP_016869465.1:p.Ser604Asn
XM_017013977.2:c.1596G>A	XP_016869466.1:p.Gln532=
XM_017013978.2:c.1548G>A	XP_016869467.1:p.Gln516=
XM_017013979.2:c.993G>A	XP_016869468.1:p.Gln331=
XM_024447332.1:c.966G>A	XP_024303100.1:p.Gln322=
XM_024447333.1:c.912G>A	XP_024303101.1:p.Gln304=
NM_145201.6:c.1592G>A MANE Select	NP_660202.3:p.Ser531Asn
NM_001286829.2:c.1553G>A	NP_001273758.1:p.Ser518Asn