Canonical Allele Identifier: CA372450668

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657596C>T (hg19) ; chr8:g.143575426C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575426C>T , CM000670.2:g.143575426C>T	GRCh38
NC_000008.10:g.144657596C>T , CM000670.1:g.144657596C>T	GRCh37
NC_000008.9:g.144728739C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1288G>A MANE Select	ENSP00000401508.2:p.Asp430Asn
ENST00000340490.7:c.1288G>A	ENSP00000341136.3:p.Asp430Asn
ENST00000426292.7:c.1288G>A	ENSP00000390949.3:p.Asp430Asn
ENST00000435154.7:c.1288G>A	ENSP00000405670.3:p.Asp430Asn
ENST00000449291.6:c.1288G>A	ENSP00000401508.2:p.Asp430Asn
ENST00000460623.5:c.266G>A
ENST00000464332.5:n.832G>A
NM_001286829.1:c.1288G>A	NP_001273758.1:p.Asp430Asn
NM_145201.5:c.1288G>A	NP_660202.3:p.Asp430Asn
XM_011517377.1:c.1288G>A	XP_011515679.1:p.Asp430Asn
NM_001363145.1:c.1207G>A	NP_001350074.1:p.Asp403Asn
NM_001363146.1:c.604G>A	NP_001350075.1:p.Asp202Asn
XM_017013975.2:c.1507G>A	XP_016869464.1:p.Asp503Asn
XM_017013976.2:c.1507G>A	XP_016869465.1:p.Asp503Asn
XM_017013977.2:c.1207G>A	XP_016869466.1:p.Asp403Asn
XM_017013978.2:c.1507G>A	XP_016869467.1:p.Asp503Asn
XM_017013979.2:c.604G>A	XP_016869468.1:p.Asp202Asn
XM_024447332.1:c.925G>A	XP_024303100.1:p.Asp309Asn
XM_024447333.1:c.523G>A	XP_024303101.1:p.Asp175Asn
NM_145201.6:c.1288G>A MANE Select	NP_660202.3:p.Asp430Asn
NM_001286829.2:c.1288G>A	NP_001273758.1:p.Asp430Asn