Canonical Allele Identifier: CA372448670

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657071C>G (hg19) ; chr8:g.143574901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574901C>G , CM000670.2:g.143574901C>G	GRCh38
NC_000008.10:g.144657071C>G , CM000670.1:g.144657071C>G	GRCh37
NC_000008.9:g.144728214C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1555-1G>C MANE Select	ENSP00000401508.2:n.1555-1G>C
ENST00000340490.7:c.1639G>C	ENSP00000341136.3:p.Gly547Arg
ENST00000426292.7:c.1516-1G>C	ENSP00000390949.3:n.1516-1G>C
ENST00000435154.7:c.*263G>C	ENSP00000405670.3:n.*263G>C
ENST00000449291.6:c.1555-1G>C	ENSP00000401508.2:n.1555-1G>C
ENST00000460623.5:c.578G>C
ENST00000464332.5:n.1099-1G>C
ENST00000498076.5:n.334-1G>C
ENST00000529179.1:n.339-1G>C
NM_001286829.1:c.1516-1G>C	NP_001273758.1:n.1516-1G>C
NM_145201.5:c.1555-1G>C	NP_660202.3:n.1555-1G>C
XM_011517377.1:c.1292-1G>C	XP_011515679.1:n.1292-1G>C
NM_001363145.1:c.1474-1G>C	NP_001350074.1:n.1474-1G>C
NM_001363146.1:c.871-1G>C	NP_001350075.1:n.871-1G>C
XM_017013975.2:c.1858G>C	XP_016869464.1:p.Gly620Arg
XM_017013976.2:c.1774-1G>C	XP_016869465.1:n.1774-1G>C
XM_017013977.2:c.1558G>C	XP_016869466.1:p.Gly520Arg
XM_017013978.2:c.1511-1G>C	XP_016869467.1:n.1511-1G>C
XM_017013979.2:c.955G>C	XP_016869468.1:p.Gly319Arg
XM_024447332.1:c.929-1G>C	XP_024303100.1:n.929-1G>C
XM_024447333.1:c.874G>C	XP_024303101.1:p.Gly292Arg
NM_145201.6:c.1555-1G>C MANE Select	NP_660202.3:n.1555-1G>C
NM_001286829.2:c.1516-1G>C	NP_001273758.1:n.1516-1G>C