Canonical Allele Identifier: CA2739973630

Gene: NAPRT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143574917A>C , CM000670.2:g.143574917A>C	GRCh38
NC_000008.10:g.144657087A>C , CM000670.1:g.144657087A>C	GRCh37
NC_000008.9:g.144728230A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1555-17T>G MANE Select	ENSP00000401508.2:n.1555-17T>G
ENST00000340490.7:c.1623T>G	ENSP00000341136.3:p.Cys541Trp
ENST00000426292.7:c.1516-17T>G	ENSP00000390949.3:n.1516-17T>G
ENST00000435154.7:c.*247T>G	ENSP00000405670.3:n.*247T>G
ENST00000449291.6:c.1555-17T>G	ENSP00000401508.2:n.1555-17T>G
ENST00000460623.5:c.562T>G
ENST00000464332.5:n.1099-17T>G
ENST00000498076.5:n.334-17T>G
ENST00000529179.1:n.339-17T>G
NM_001286829.1:c.1516-17T>G	NP_001273758.1:n.1516-17T>G
NM_145201.5:c.1555-17T>G	NP_660202.3:n.1555-17T>G
XM_011517377.1:c.1292-17T>G	XP_011515679.1:n.1292-17T>G
NM_001363145.1:c.1474-17T>G	NP_001350074.1:n.1474-17T>G
NM_001363146.1:c.871-17T>G	NP_001350075.1:n.871-17T>G
XM_017013975.2:c.1842T>G	XP_016869464.1:p.Cys614Trp
XM_017013976.2:c.1774-17T>G	XP_016869465.1:n.1774-17T>G
XM_017013977.2:c.1542T>G	XP_016869466.1:p.Cys514Trp
XM_017013978.2:c.1511-17T>G	XP_016869467.1:n.1511-17T>G
XM_017013979.2:c.939T>G	XP_016869468.1:p.Cys313Trp
XM_024447332.1:c.929-17T>G	XP_024303100.1:n.929-17T>G
XM_024447333.1:c.858T>G	XP_024303101.1:p.Cys286Trp
NM_145201.6:c.1555-17T>G MANE Select	NP_660202.3:n.1555-17T>G
NM_001286829.2:c.1516-17T>G	NP_001273758.1:n.1516-17T>G