Canonical Allele Identifier: CA463511621

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657183C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575013C>T , CM000670.2:g.143575013C>T	GRCh38
NC_000008.10:g.144657183C>T , CM000670.1:g.144657183C>T	GRCh37
NC_000008.9:g.144728326C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1527G>A MANE Select	ENSP00000401508.2:p.Arg509=
ENST00000340490.7:c.1527G>A	ENSP00000341136.3:p.Arg509=
ENST00000426292.7:c.1488G>A	ENSP00000390949.3:p.Arg496=
ENST00000435154.7:c.*151G>A	ENSP00000405670.3:n.*151G>A
ENST00000449291.6:c.1527G>A	ENSP00000401508.2:p.Arg509=
ENST00000460623.5:c.466G>A
ENST00000464332.5:n.1071G>A
ENST00000498076.5:n.306G>A
ENST00000529179.1:n.311G>A
NM_001286829.1:c.1488G>A	NP_001273758.1:p.Arg496=
NM_145201.5:c.1527G>A	NP_660202.3:p.Arg509=
XM_011517377.1:c.1292-113G>A	XP_011515679.1:n.1292-113G>A
NM_001363145.1:c.1446G>A	NP_001350074.1:p.Arg482=
NM_001363146.1:c.843G>A	NP_001350075.1:p.Arg281=
XM_017013975.2:c.1746G>A	XP_016869464.1:p.Arg582=
XM_017013976.2:c.1746G>A	XP_016869465.1:p.Arg582=
XM_017013977.2:c.1446G>A	XP_016869466.1:p.Arg482=
XM_017013978.2:c.1511-113G>A	XP_016869467.1:n.1511-113G>A
XM_017013979.2:c.843G>A	XP_016869468.1:p.Arg281=
XM_024447332.1:c.929-113G>A	XP_024303100.1:n.929-113G>A
XM_024447333.1:c.762G>A	XP_024303101.1:p.Arg254=
NM_145201.6:c.1527G>A MANE Select	NP_660202.3:p.Arg509=
NM_001286829.2:c.1488G>A	NP_001273758.1:p.Arg496=