Canonical Allele Identifier: CA2200859699

Gene: NPRL3

Linked Data

• dbSNP Id: rs1899907689

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.113546_113558del , CM000678.2:g.113546_113558del	GRCh38
NC_000016.9:g.163545_163557del , CM000678.1:g.163545_163557del	GRCh37
NC_000016.8:g.103545_103557del	NCBI36
NG_029669.1:g.30142_30154del

Transcript Alleles

HGVS	Amino-acid change
ENST00000611875.5:c.394-782_394-770del MANE Select	ENSP00000478273.1:n.394-782_394-770del
ENST00000399953.7:c.319-782_319-770del	ENSP00000382834.4:n.319-782_319-770del
ENST00000419636.1:c.433-782_433-770del	ENSP00000399894.1:n.433-782_433-770del
ENST00000422814.5:c.37-782_37-770del	ENSP00000395288.1:n.37-782_37-770del
ENST00000456528.5:c.*195-782_*195-770del	ENSP00000401529.1:n.*195-782_*195-770del
ENST00000457916.5:c.*135-782_*135-770del	ENSP00000405942.1:n.*135-782_*135-770del
ENST00000468260.5:c.160-782_160-770del	ENSP00000477764.1:n.160-782_160-770del
ENST00000473674.5:n.258-782_258-770del
ENST00000483663.5:c.*135-782_*135-770del	ENSP00000418475.1:n.*135-782_*135-770del
ENST00000611875.4:c.394-782_394-770del	ENSP00000478273.1:n.394-782_394-770del
ENST00000620134.4:c.394-782_394-770del	ENSP00000483814.1:n.394-782_394-770del
ENST00000621703.4:c.189-782_189-770del	ENSP00000477801.1:n.189-782_189-770del
ENST00000622194.4:c.*30-782_*30-770del	ENSP00000478045.1:n.*30-782_*30-770del
NM_001039476.2:c.-144-782_-144-770del	NP_001034565.1:n.-144-782_-144-770del
NM_001077350.2:c.394-782_394-770del	NP_001070818.1:n.394-782_394-770del
NM_001243247.1:c.160-782_160-770del	NP_001230176.1:n.160-782_160-770del
NM_001243248.1:c.319-782_319-770del	NP_001230177.1:n.319-782_319-770del
NM_001243249.1:c.319-782_319-770del	NP_001230178.1:n.319-782_319-770del
XM_011522668.1:c.433-782_433-770del	XP_011520970.1:n.433-782_433-770del
XM_011522669.1:c.394-782_394-770del	XP_011520971.1:n.394-782_394-770del
XM_011522670.1:c.394-782_394-770del	XP_011520972.1:n.394-782_394-770del
XM_011522671.1:c.358-782_358-770del	XP_011520973.1:n.358-782_358-770del
XM_011522672.1:c.319-782_319-770del	XP_011520974.1:n.319-782_319-770del
XM_011522673.1:c.319-782_319-770del	XP_011520975.1:n.319-782_319-770del
XM_011522674.1:c.319-782_319-770del	XP_011520976.1:n.319-782_319-770del
XM_011522675.1:c.160-782_160-770del	XP_011520977.1:n.160-782_160-770del
XM_011522676.1:c.160-782_160-770del	XP_011520978.1:n.160-782_160-770del
XM_011522677.1:c.160-782_160-770del	XP_011520979.1:n.160-782_160-770del
XM_011522678.1:c.-144-782_-144-770del	XP_011520980.1:n.-144-782_-144-770del
XM_011522679.1:c.-144-782_-144-770del	XP_011520981.1:n.-144-782_-144-770del
XM_011522680.1:c.-144-782_-144-770del	XP_011520982.1:n.-144-782_-144-770del
XM_011522681.1:c.-144-782_-144-770del	XP_011520983.1:n.-144-782_-144-770del
NM_001077350.3:c.394-782_394-770del MANE Select	NP_001070818.1:n.394-782_394-770del
NM_001039476.3:c.-144-782_-144-770del	NP_001034565.1:n.-144-782_-144-770del
NM_001243247.2:c.160-782_160-770del	NP_001230176.1:n.160-782_160-770del
NM_001243248.2:c.319-782_319-770del	NP_001230177.1:n.319-782_319-770del
NM_001243249.2:c.319-782_319-770del	NP_001230178.1:n.319-782_319-770del