Canonical Allele Identifier: CA645604803

Gene: UPF3B

Linked Data

• COSMIC: COSM5611549

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119841223_119841224delinsTT , CM000685.2:g.119841223_119841224delinsTT	GRCh38
NC_000023.10:g.118975186_118975187delinsTT , CM000685.1:g.118975186_118975187delinsTT	GRCh37
NC_000023.9:g.118859214_118859215delinsTT	NCBI36
NG_009241.1:g.16782_16783delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276201.7:c.659_660delinsAA MANE Select	ENSP00000276201.3:p.Arg220Lys
ENST00000276201.6:c.659_660delinsAA	ENSP00000276201.2:p.Arg220Lys
ENST00000345865.6:c.659_660delinsAA	ENSP00000245418.2:p.Arg220Lys
ENST00000478840.1:n.247_248delinsAA
ENST00000619445.1:c.624+511_624+512delinsAA	ENSP00000481698.1:n.624+511_624+512delinsAA
NM_023010.3:c.659_660delinsAA	NP_075386.1:p.Arg220Lys
NM_080632.2:c.659_660delinsAA	NP_542199.1:p.Arg220Lys
XM_005262458.3:c.659_660delinsAA	XP_005262515.1:p.Arg220Lys
XM_006724780.2:c.659_660delinsAA	XP_006724843.1:p.Arg220Lys
XM_006724781.2:c.659_660delinsAA	XP_006724844.1:p.Arg220Lys
XM_011531378.1:c.659_660delinsAA	XP_011529680.1:p.Arg220Lys
XM_011531379.1:c.659_660delinsAA	XP_011529681.1:p.Arg220Lys
XM_017029737.1:c.659_660delinsAA	XP_016885226.1:p.Arg220Lys
XM_017029738.1:c.659_660delinsAA	XP_016885227.1:p.Arg220Lys
XM_017029739.1:c.659_660delinsAA	XP_016885228.1:p.Arg220Lys
XM_017029740.1:c.659_660delinsAA	XP_016885229.1:p.Arg220Lys
NM_080632.3:c.659_660delinsAA MANE Select	NP_542199.1:p.Arg220Lys
NM_023010.4:c.659_660delinsAA	NP_075386.1:p.Arg220Lys