Canonical Allele Identifier: CA463511655

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657210G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575040G>T , CM000670.2:g.143575040G>T	GRCh38
NC_000008.10:g.144657210G>T , CM000670.1:g.144657210G>T	GRCh37
NC_000008.9:g.144728353G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1500C>A MANE Select	ENSP00000401508.2:p.Ser500=
ENST00000340490.7:c.1500C>A	ENSP00000341136.3:p.Ser500=
ENST00000426292.7:c.1461C>A	ENSP00000390949.3:p.Ser487=
ENST00000435154.7:c.*124C>A	ENSP00000405670.3:n.*124C>A
ENST00000449291.6:c.1500C>A	ENSP00000401508.2:p.Ser500=
ENST00000460623.5:c.439C>A
ENST00000464332.5:n.1044C>A
ENST00000498076.5:n.279C>A
ENST00000529179.1:n.284C>A
NM_001286829.1:c.1461C>A	NP_001273758.1:p.Ser487=
NM_145201.5:c.1500C>A	NP_660202.3:p.Ser500=
XM_011517377.1:c.1292-140C>A	XP_011515679.1:n.1292-140C>A
NM_001363145.1:c.1419C>A	NP_001350074.1:p.Ser473=
NM_001363146.1:c.816C>A	NP_001350075.1:p.Ser272=
XM_017013975.2:c.1719C>A	XP_016869464.1:p.Ser573=
XM_017013976.2:c.1719C>A	XP_016869465.1:p.Ser573=
XM_017013977.2:c.1419C>A	XP_016869466.1:p.Ser473=
XM_017013978.2:c.1511-140C>A	XP_016869467.1:n.1511-140C>A
XM_017013979.2:c.816C>A	XP_016869468.1:p.Ser272=
XM_024447332.1:c.929-140C>A	XP_024303100.1:n.929-140C>A
XM_024447333.1:c.735C>A	XP_024303101.1:p.Ser245=
NM_145201.6:c.1500C>A MANE Select	NP_660202.3:p.Ser500=
NM_001286829.2:c.1461C>A	NP_001273758.1:p.Ser487=