Canonical Allele Identifier: CA372448494

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657035G>T (hg19) ; chr8:g.143574865G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574865G>T , CM000670.2:g.143574865G>T	GRCh38
NC_000008.10:g.144657035G>T , CM000670.1:g.144657035G>T	GRCh37
NC_000008.9:g.144728178G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1590C>A MANE Select	ENSP00000401508.2:p.Asn530Lys
ENST00000340490.7:c.1675C>A	ENSP00000341136.3:p.Gln559Lys
ENST00000426292.7:c.1551C>A	ENSP00000390949.3:p.Asn517Lys
ENST00000435154.7:c.*299C>A	ENSP00000405670.3:n.*299C>A
ENST00000449291.6:c.1590C>A	ENSP00000401508.2:p.Asn530Lys
ENST00000460623.5:c.614C>A
ENST00000464332.5:n.1134C>A
ENST00000498076.5:n.369C>A
ENST00000529179.1:n.374C>A
NM_001286829.1:c.1551C>A	NP_001273758.1:p.Asn517Lys
NM_145201.5:c.1590C>A	NP_660202.3:p.Asn530Lys
XM_011517377.1:c.1327C>A	XP_011515679.1:p.Gln443Lys
NM_001363145.1:c.1509C>A	NP_001350074.1:p.Asn503Lys
NM_001363146.1:c.906C>A	NP_001350075.1:p.Asn302Lys
XM_017013975.2:c.1894C>A	XP_016869464.1:p.Gln632Lys
XM_017013976.2:c.1809C>A	XP_016869465.1:p.Asn603Lys
XM_017013977.2:c.1594C>A	XP_016869466.1:p.Gln532Lys
XM_017013978.2:c.1546C>A	XP_016869467.1:p.Gln516Lys
XM_017013979.2:c.991C>A	XP_016869468.1:p.Gln331Lys
XM_024447332.1:c.964C>A	XP_024303100.1:p.Gln322Lys
XM_024447333.1:c.910C>A	XP_024303101.1:p.Gln304Lys
NM_145201.6:c.1590C>A MANE Select	NP_660202.3:p.Asn530Lys
NM_001286829.2:c.1551C>A	NP_001273758.1:p.Asn517Lys