Canonical Allele Identifier: CA2688943461

Gene: NAPRT

Linked Data

• gnomAD v4: 8-143575134-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143575137del , CM000670.2:g.143575137del	GRCh38
NC_000008.10:g.144657307del , CM000670.1:g.144657307del	GRCh37
NC_000008.9:g.144728450del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449291.7:c.1447-42del MANE Select	ENSP00000401508.2:n.1447-42del
ENST00000340490.7:c.1447-42del	ENSP00000341136.3:n.1447-42del
ENST00000426292.7:c.1408-42del	ENSP00000390949.3:n.1408-42del
ENST00000435154.7:c.*29del	ENSP00000405670.3:n.*29del
ENST00000449291.6:c.1447-42del	ENSP00000401508.2:n.1447-42del
ENST00000460623.5:c.386-42del
ENST00000464332.5:n.991-42del
ENST00000498076.5:n.226-42del
ENST00000529179.1:n.189del
NM_001286829.1:c.1408-42del	NP_001273758.1:n.1408-42del
NM_145201.5:c.1447-42del	NP_660202.3:n.1447-42del
XM_011517377.1:c.1292-235del	XP_011515679.1:n.1292-235del
NM_001363145.1:c.1366-42del	NP_001350074.1:n.1366-42del
NM_001363146.1:c.763-42del	NP_001350075.1:n.763-42del
XM_017013975.2:c.1666-42del	XP_016869464.1:n.1666-42del
XM_017013976.2:c.1666-42del	XP_016869465.1:n.1666-42del
XM_017013977.2:c.1366-42del	XP_016869466.1:n.1366-42del
XM_017013978.2:c.1511-235del	XP_016869467.1:n.1511-235del
XM_017013979.2:c.763-42del	XP_016869468.1:n.763-42del
XM_024447332.1:c.929-235del	XP_024303100.1:n.929-235del
XM_024447333.1:c.682-42del	XP_024303101.1:n.682-42del
NM_145201.6:c.1447-42del MANE Select	NP_660202.3:n.1447-42del
NM_001286829.2:c.1408-42del	NP_001273758.1:n.1408-42del