Canonical Allele Identifier: CA372448537

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657045G>C (hg19) ; chr8:g.143574875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574875G>C , CM000670.2:g.143574875G>C	GRCh38
NC_000008.10:g.144657045G>C , CM000670.1:g.144657045G>C	GRCh37
NC_000008.9:g.144728188G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1580C>G MANE Select	ENSP00000401508.2:p.Ala527Gly
ENST00000340490.7:c.1665C>G	ENSP00000341136.3:p.Gly555=
ENST00000426292.7:c.1541C>G	ENSP00000390949.3:p.Ala514Gly
ENST00000435154.7:c.*289C>G	ENSP00000405670.3:n.*289C>G
ENST00000449291.6:c.1580C>G	ENSP00000401508.2:p.Ala527Gly
ENST00000460623.5:c.604C>G
ENST00000464332.5:n.1124C>G
ENST00000498076.5:n.359C>G
ENST00000529179.1:n.364C>G
NM_001286829.1:c.1541C>G	NP_001273758.1:p.Ala514Gly
NM_145201.5:c.1580C>G	NP_660202.3:p.Ala527Gly
XM_011517377.1:c.1317C>G	XP_011515679.1:p.Gly439=
NM_001363145.1:c.1499C>G	NP_001350074.1:p.Ala500Gly
NM_001363146.1:c.896C>G	NP_001350075.1:p.Ala299Gly
XM_017013975.2:c.1884C>G	XP_016869464.1:p.Gly628=
XM_017013976.2:c.1799C>G	XP_016869465.1:p.Ala600Gly
XM_017013977.2:c.1584C>G	XP_016869466.1:p.Gly528=
XM_017013978.2:c.1536C>G	XP_016869467.1:p.Gly512=
XM_017013979.2:c.981C>G	XP_016869468.1:p.Gly327=
XM_024447332.1:c.954C>G	XP_024303100.1:p.Gly318=
XM_024447333.1:c.900C>G	XP_024303101.1:p.Gly300=
NM_145201.6:c.1580C>G MANE Select	NP_660202.3:p.Ala527Gly
NM_001286829.2:c.1541C>G	NP_001273758.1:p.Ala514Gly