Canonical Allele Identifier: CA372451156

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657645C>G (hg19) ; chr8:g.143575475C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575475C>G , CM000670.2:g.143575475C>G	GRCh38
NC_000008.10:g.144657645C>G , CM000670.1:g.144657645C>G	GRCh37
NC_000008.9:g.144728788C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1239G>C MANE Select	ENSP00000401508.2:p.Glu413Asp
ENST00000340490.7:c.1239G>C	ENSP00000341136.3:p.Glu413Asp
ENST00000426292.7:c.1239G>C	ENSP00000390949.3:p.Glu413Asp
ENST00000435154.7:c.1239G>C	ENSP00000405670.3:p.Glu413Asp
ENST00000449291.6:c.1239G>C	ENSP00000401508.2:p.Glu413Asp
ENST00000460623.5:c.217G>C
ENST00000464332.5:n.783G>C
ENST00000525583.5:c.1023G>C
NM_001286829.1:c.1239G>C	NP_001273758.1:p.Glu413Asp
NM_145201.5:c.1239G>C	NP_660202.3:p.Glu413Asp
XM_011517377.1:c.1239G>C	XP_011515679.1:p.Glu413Asp
NM_001363145.1:c.1158G>C	NP_001350074.1:p.Glu386Asp
NM_001363146.1:c.555G>C	NP_001350075.1:p.Glu185Asp
XM_017013975.2:c.1458G>C	XP_016869464.1:p.Glu486Asp
XM_017013976.2:c.1458G>C	XP_016869465.1:p.Glu486Asp
XM_017013977.2:c.1158G>C	XP_016869466.1:p.Glu386Asp
XM_017013978.2:c.1458G>C	XP_016869467.1:p.Glu486Asp
XM_017013979.2:c.555G>C	XP_016869468.1:p.Glu185Asp
XM_024447332.1:c.876G>C	XP_024303100.1:p.Glu292Asp
XM_024447333.1:c.474G>C	XP_024303101.1:p.Glu158Asp
NM_145201.6:c.1239G>C MANE Select	NP_660202.3:p.Glu413Asp
NM_001286829.2:c.1239G>C	NP_001273758.1:p.Glu413Asp