Canonical Allele Identifier: CA2579271882

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575351T>C , CM000670.2:g.143575351T>C	GRCh38
NC_000008.10:g.144657521T>C , CM000670.1:g.144657521T>C	GRCh37
NC_000008.9:g.144728664T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1292-6A>G MANE Select	ENSP00000401508.2:n.1292-6A>G
ENST00000340490.7:c.1292-6A>G	ENSP00000341136.3:n.1292-6A>G
ENST00000426292.7:c.1292-6A>G	ENSP00000390949.3:n.1292-6A>G
ENST00000435154.7:c.1292-6A>G	ENSP00000405670.3:n.1292-6A>G
ENST00000449291.6:c.1292-6A>G	ENSP00000401508.2:n.1292-6A>G
ENST00000460623.5:c.270-6A>G
ENST00000464332.5:n.836-6A>G
ENST00000498076.5:n.65A>G
NM_001286829.1:c.1292-6A>G	NP_001273758.1:n.1292-6A>G
NM_145201.5:c.1292-6A>G	NP_660202.3:n.1292-6A>G
XM_011517377.1:c.1291+72A>G	XP_011515679.1:n.1291+72A>G
NM_001363145.1:c.1211-6A>G	NP_001350074.1:n.1211-6A>G
NM_001363146.1:c.608-6A>G	NP_001350075.1:n.608-6A>G
XM_017013975.2:c.1511-6A>G	XP_016869464.1:n.1511-6A>G
XM_017013976.2:c.1511-6A>G	XP_016869465.1:n.1511-6A>G
XM_017013977.2:c.1211-6A>G	XP_016869466.1:n.1211-6A>G
XM_017013978.2:c.1510+72A>G	XP_016869467.1:n.1510+72A>G
XM_017013979.2:c.608-6A>G	XP_016869468.1:n.608-6A>G
XM_024447332.1:c.928+72A>G	XP_024303100.1:n.928+72A>G
XM_024447333.1:c.527-6A>G	XP_024303101.1:n.527-6A>G
NM_145201.6:c.1292-6A>G MANE Select	NP_660202.3:n.1292-6A>G
NM_001286829.2:c.1292-6A>G	NP_001273758.1:n.1292-6A>G