Canonical Allele Identifier: CA463511657

Gene: NAPRT

Linked Data

• gnomAD v4: 8-143575043-C-A
• MyVariant Identifiers: chr8:g.144657213C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575043C>A , CM000670.2:g.143575043C>A	GRCh38
NC_000008.10:g.144657213C>A , CM000670.1:g.144657213C>A	GRCh37
NC_000008.9:g.144728356C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1497G>T MANE Select	ENSP00000401508.2:p.Leu499=
ENST00000340490.7:c.1497G>T	ENSP00000341136.3:p.Leu499=
ENST00000426292.7:c.1458G>T	ENSP00000390949.3:p.Leu486=
ENST00000435154.7:c.*121G>T	ENSP00000405670.3:n.*121G>T
ENST00000449291.6:c.1497G>T	ENSP00000401508.2:p.Leu499=
ENST00000460623.5:c.436G>T
ENST00000464332.5:n.1041G>T
ENST00000498076.5:n.276G>T
ENST00000529179.1:n.281G>T
NM_001286829.1:c.1458G>T	NP_001273758.1:p.Leu486=
NM_145201.5:c.1497G>T	NP_660202.3:p.Leu499=
XM_011517377.1:c.1292-143G>T	XP_011515679.1:n.1292-143G>T
NM_001363145.1:c.1416G>T	NP_001350074.1:p.Leu472=
NM_001363146.1:c.813G>T	NP_001350075.1:p.Leu271=
XM_017013975.2:c.1716G>T	XP_016869464.1:p.Leu572=
XM_017013976.2:c.1716G>T	XP_016869465.1:p.Leu572=
XM_017013977.2:c.1416G>T	XP_016869466.1:p.Leu472=
XM_017013978.2:c.1511-143G>T	XP_016869467.1:n.1511-143G>T
XM_017013979.2:c.813G>T	XP_016869468.1:p.Leu271=
XM_024447332.1:c.929-143G>T	XP_024303100.1:n.929-143G>T
XM_024447333.1:c.732G>T	XP_024303101.1:p.Leu244=
NM_145201.6:c.1497G>T MANE Select	NP_660202.3:p.Leu499=
NM_001286829.2:c.1458G>T	NP_001273758.1:p.Leu486=