Canonical Allele Identifier: CA848762776

Gene: NAPRT

Linked Data

• dbSNP Id: rs77951814
• gnomAD v3: 8-143574982-C-A
• gnomAD v4: 8-143574982-C-A
• MyVariant Identifiers: chr8:g.144657152C>A (hg19) ; chr8:g.143574982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574982C>A , CM000670.2:g.143574982C>A	GRCh38
NC_000008.10:g.144657152C>A , CM000670.1:g.144657152C>A	GRCh37
NC_000008.9:g.144728295C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1554+4G>T MANE Select	ENSP00000401508.2:n.1554+4G>T
ENST00000340490.7:c.1558G>T	ENSP00000341136.3:p.Gly520Trp
ENST00000426292.7:c.1515+4G>T	ENSP00000390949.3:n.1515+4G>T
ENST00000435154.7:c.*182G>T	ENSP00000405670.3:n.*182G>T
ENST00000449291.6:c.1554+4G>T	ENSP00000401508.2:n.1554+4G>T
ENST00000460623.5:c.497G>T
ENST00000464332.5:n.1098+4G>T
ENST00000498076.5:n.333+4G>T
ENST00000529179.1:n.338+4G>T
NM_001286829.1:c.1515+4G>T	NP_001273758.1:n.1515+4G>T
NM_145201.5:c.1554+4G>T	NP_660202.3:n.1554+4G>T
XM_011517377.1:c.1292-82G>T	XP_011515679.1:n.1292-82G>T
NM_001363145.1:c.1473+4G>T	NP_001350074.1:n.1473+4G>T
NM_001363146.1:c.870+4G>T	NP_001350075.1:n.870+4G>T
XM_017013975.2:c.1777G>T	XP_016869464.1:p.Gly593Trp
XM_017013976.2:c.1773+4G>T	XP_016869465.1:n.1773+4G>T
XM_017013977.2:c.1477G>T	XP_016869466.1:p.Gly493Trp
XM_017013978.2:c.1511-82G>T	XP_016869467.1:n.1511-82G>T
XM_017013979.2:c.874G>T	XP_016869468.1:p.Gly292Trp
XM_024447332.1:c.929-82G>T	XP_024303100.1:n.929-82G>T
XM_024447333.1:c.793G>T	XP_024303101.1:p.Gly265Trp
NM_145201.6:c.1554+4G>T MANE Select	NP_660202.3:n.1554+4G>T
NM_001286829.2:c.1515+4G>T	NP_001273758.1:n.1515+4G>T