Canonical Allele Identifier: CA372449898

Gene: NAPRT

Linked Data

• MyVariant Identifiers: chr8:g.144657408G>C (hg19) ; chr8:g.143575238G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575238G>C , CM000670.2:g.143575238G>C	GRCh38
NC_000008.10:g.144657408G>C , CM000670.1:g.144657408G>C	GRCh37
NC_000008.9:g.144728551G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1399C>G MANE Select	ENSP00000401508.2:p.Pro467Ala
ENST00000340490.7:c.1399C>G	ENSP00000341136.3:p.Pro467Ala
ENST00000426292.7:c.1399C>G	ENSP00000390949.3:p.Pro467Ala
ENST00000435154.7:c.1399C>G	ENSP00000405670.3:p.Pro467Ala
ENST00000449291.6:c.1399C>G	ENSP00000401508.2:p.Pro467Ala
ENST00000460623.5:c.377C>G
ENST00000464332.5:n.943C>G
ENST00000498076.5:n.178C>G
ENST00000529179.1:n.86C>G
NM_001286829.1:c.1399C>G	NP_001273758.1:p.Pro467Ala
NM_145201.5:c.1399C>G	NP_660202.3:p.Pro467Ala
XM_011517377.1:c.1291+185C>G	XP_011515679.1:n.1291+185C>G
NM_001363145.1:c.1318C>G	NP_001350074.1:p.Pro440Ala
NM_001363146.1:c.715C>G	NP_001350075.1:p.Pro239Ala
XM_017013975.2:c.1618C>G	XP_016869464.1:p.Pro540Ala
XM_017013976.2:c.1618C>G	XP_016869465.1:p.Pro540Ala
XM_017013977.2:c.1318C>G	XP_016869466.1:p.Pro440Ala
XM_017013978.2:c.1510+185C>G	XP_016869467.1:n.1510+185C>G
XM_017013979.2:c.715C>G	XP_016869468.1:p.Pro239Ala
XM_024447332.1:c.928+185C>G	XP_024303100.1:n.928+185C>G
XM_024447333.1:c.634C>G	XP_024303101.1:p.Pro212Ala
NM_145201.6:c.1399C>G MANE Select	NP_660202.3:p.Pro467Ala
NM_001286829.2:c.1399C>G	NP_001273758.1:p.Pro467Ala