Canonical Allele Identifier: CA372448579

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657053C>G (hg19) ; chr8:g.143574883C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574883C>G , CM000670.2:g.143574883C>G	GRCh38
NC_000008.10:g.144657053C>G , CM000670.1:g.144657053C>G	GRCh37
NC_000008.9:g.144728196C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1572G>C MANE Select	ENSP00000401508.2:p.Arg524Ser
ENST00000340490.7:c.1657G>C	ENSP00000341136.3:p.Ala553Pro
ENST00000426292.7:c.1533G>C	ENSP00000390949.3:p.Arg511Ser
ENST00000435154.7:c.*281G>C	ENSP00000405670.3:n.*281G>C
ENST00000449291.6:c.1572G>C	ENSP00000401508.2:p.Arg524Ser
ENST00000460623.5:c.596G>C
ENST00000464332.5:n.1116G>C
ENST00000498076.5:n.351G>C
ENST00000529179.1:n.356G>C
NM_001286829.1:c.1533G>C	NP_001273758.1:p.Arg511Ser
NM_145201.5:c.1572G>C	NP_660202.3:p.Arg524Ser
XM_011517377.1:c.1309G>C	XP_011515679.1:p.Ala437Pro
NM_001363145.1:c.1491G>C	NP_001350074.1:p.Arg497Ser
NM_001363146.1:c.888G>C	NP_001350075.1:p.Arg296Ser
XM_017013975.2:c.1876G>C	XP_016869464.1:p.Ala626Pro
XM_017013976.2:c.1791G>C	XP_016869465.1:p.Arg597Ser
XM_017013977.2:c.1576G>C	XP_016869466.1:p.Ala526Pro
XM_017013978.2:c.1528G>C	XP_016869467.1:p.Ala510Pro
XM_017013979.2:c.973G>C	XP_016869468.1:p.Ala325Pro
XM_024447332.1:c.946G>C	XP_024303100.1:p.Ala316Pro
XM_024447333.1:c.892G>C	XP_024303101.1:p.Ala298Pro
NM_145201.6:c.1572G>C MANE Select	NP_660202.3:p.Arg524Ser
NM_001286829.2:c.1533G>C	NP_001273758.1:p.Arg511Ser