Canonical Allele Identifier: CA372449031

Gene: NAPRT

Linked Data

• gnomAD v4: 8-143575050-G-A
• MyVariant Identifiers: chr8:g.144657220G>A (hg19) ; chr8:g.143575050G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575050G>A , CM000670.2:g.143575050G>A	GRCh38
NC_000008.10:g.144657220G>A , CM000670.1:g.144657220G>A	GRCh37
NC_000008.9:g.144728363G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1490C>T MANE Select	ENSP00000401508.2:p.Ala497Val
ENST00000340490.7:c.1490C>T	ENSP00000341136.3:p.Ala497Val
ENST00000426292.7:c.1451C>T	ENSP00000390949.3:p.Ala484Val
ENST00000435154.7:c.*114C>T	ENSP00000405670.3:n.*114C>T
ENST00000449291.6:c.1490C>T	ENSP00000401508.2:p.Ala497Val
ENST00000460623.5:c.429C>T
ENST00000464332.5:n.1034C>T
ENST00000498076.5:n.269C>T
ENST00000529179.1:n.274C>T
NM_001286829.1:c.1451C>T	NP_001273758.1:p.Ala484Val
NM_145201.5:c.1490C>T	NP_660202.3:p.Ala497Val
XM_011517377.1:c.1292-150C>T	XP_011515679.1:n.1292-150C>T
NM_001363145.1:c.1409C>T	NP_001350074.1:p.Ala470Val
NM_001363146.1:c.806C>T	NP_001350075.1:p.Ala269Val
XM_017013975.2:c.1709C>T	XP_016869464.1:p.Ala570Val
XM_017013976.2:c.1709C>T	XP_016869465.1:p.Ala570Val
XM_017013977.2:c.1409C>T	XP_016869466.1:p.Ala470Val
XM_017013978.2:c.1511-150C>T	XP_016869467.1:n.1511-150C>T
XM_017013979.2:c.806C>T	XP_016869468.1:p.Ala269Val
XM_024447332.1:c.929-150C>T	XP_024303100.1:n.929-150C>T
XM_024447333.1:c.725C>T	XP_024303101.1:p.Ala242Val
NM_145201.6:c.1490C>T MANE Select	NP_660202.3:p.Ala497Val
NM_001286829.2:c.1451C>T	NP_001273758.1:p.Ala484Val