Canonical Allele Identifier: CA372449893

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657405C>A (hg19) ; chr8:g.143575235C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575235C>A , CM000670.2:g.143575235C>A	GRCh38
NC_000008.10:g.144657405C>A , CM000670.1:g.144657405C>A	GRCh37
NC_000008.9:g.144728548C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000449291.7:c.1402G>T MANE Select	ENSP00000401508.2:p.Ala468Ser
ENST00000340490.7:c.1402G>T	ENSP00000341136.3:p.Ala468Ser
ENST00000426292.7:c.1402G>T	ENSP00000390949.3:p.Ala468Ser
ENST00000435154.7:c.1402G>T	ENSP00000405670.3:p.Ala468Ser
ENST00000449291.6:c.1402G>T	ENSP00000401508.2:p.Ala468Ser
ENST00000460623.5:c.380G>T
ENST00000464332.5:n.946G>T
ENST00000498076.5:n.181G>T
ENST00000529179.1:n.89G>T
NM_001286829.1:c.1402G>T	NP_001273758.1:p.Ala468Ser
NM_145201.5:c.1402G>T	NP_660202.3:p.Ala468Ser
XM_011517377.1:c.1291+188G>T	XP_011515679.1:n.1291+188G>T
NM_001363145.1:c.1321G>T	NP_001350074.1:p.Ala441Ser
NM_001363146.1:c.718G>T	NP_001350075.1:p.Ala240Ser
XM_017013975.2:c.1621G>T	XP_016869464.1:p.Ala541Ser
XM_017013976.2:c.1621G>T	XP_016869465.1:p.Ala541Ser
XM_017013977.2:c.1321G>T	XP_016869466.1:p.Ala441Ser
XM_017013978.2:c.1510+188G>T	XP_016869467.1:n.1510+188G>T
XM_017013979.2:c.718G>T	XP_016869468.1:p.Ala240Ser
XM_024447332.1:c.928+188G>T	XP_024303100.1:n.928+188G>T
XM_024447333.1:c.637G>T	XP_024303101.1:p.Ala213Ser
NM_145201.6:c.1402G>T MANE Select	NP_660202.3:p.Ala468Ser
NM_001286829.2:c.1402G>T	NP_001273758.1:p.Ala468Ser