Canonical Allele Identifier: CA585729346

Gene: NAPRT

Linked Data

• dbSNP Id: rs1433059855
• gnomAD v2: 8-144657115-G-A
• gnomAD v4: 8-143574945-G-A
• MyVariant Identifiers: chr8:g.144657115G>A (hg19) ; chr8:g.143574945G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574945G>A , CM000670.2:g.143574945G>A	GRCh38
NC_000008.10:g.144657115G>A , CM000670.1:g.144657115G>A	GRCh37
NC_000008.9:g.144728258G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1554+41C>T MANE Select	ENSP00000401508.2:n.1554+41C>T
ENST00000340490.7:c.1595C>T	ENSP00000341136.3:p.Pro532Leu
ENST00000426292.7:c.1515+41C>T	ENSP00000390949.3:n.1515+41C>T
ENST00000435154.7:c.*219C>T	ENSP00000405670.3:n.*219C>T
ENST00000449291.6:c.1554+41C>T	ENSP00000401508.2:n.1554+41C>T
ENST00000460623.5:c.534C>T
ENST00000464332.5:n.1098+41C>T
ENST00000498076.5:n.333+41C>T
ENST00000529179.1:n.338+41C>T
NM_001286829.1:c.1515+41C>T	NP_001273758.1:n.1515+41C>T
NM_145201.5:c.1554+41C>T	NP_660202.3:n.1554+41C>T
XM_011517377.1:c.1292-45C>T	XP_011515679.1:n.1292-45C>T
NM_001363145.1:c.1473+41C>T	NP_001350074.1:n.1473+41C>T
NM_001363146.1:c.870+41C>T	NP_001350075.1:n.870+41C>T
XM_017013975.2:c.1814C>T	XP_016869464.1:p.Pro605Leu
XM_017013976.2:c.1773+41C>T	XP_016869465.1:n.1773+41C>T
XM_017013977.2:c.1514C>T	XP_016869466.1:p.Pro505Leu
XM_017013978.2:c.1511-45C>T	XP_016869467.1:n.1511-45C>T
XM_017013979.2:c.911C>T	XP_016869468.1:p.Pro304Leu
XM_024447332.1:c.929-45C>T	XP_024303100.1:n.929-45C>T
XM_024447333.1:c.830C>T	XP_024303101.1:p.Pro277Leu
NM_145201.6:c.1554+41C>T MANE Select	NP_660202.3:n.1554+41C>T
NM_001286829.2:c.1515+41C>T	NP_001273758.1:n.1515+41C>T