Canonical Allele Identifier: CA518216219

Gene: UPF3B

Linked Data

• COSMIC: COSM286359
• MyVariant Identifiers: chrX:g.118975229G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119841266G>T , CM000685.2:g.119841266G>T	GRCh38
NC_000023.10:g.118975229G>T , CM000685.1:g.118975229G>T	GRCh37
NC_000023.9:g.118859257G>T	NCBI36
NG_009241.1:g.16740C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276201.7:c.625-8C>A MANE Select	ENSP00000276201.3:n.625-8C>A
ENST00000276201.6:c.625-8C>A	ENSP00000276201.2:n.625-8C>A
ENST00000345865.6:c.625-8C>A	ENSP00000245418.2:n.625-8C>A
ENST00000478840.1:n.213-8C>A
ENST00000619445.1:c.624+469C>A	ENSP00000481698.1:n.624+469C>A
NM_023010.3:c.625-8C>A	NP_075386.1:n.625-8C>A
NM_080632.2:c.625-8C>A	NP_542199.1:n.625-8C>A
XM_005262458.3:c.625-8C>A	XP_005262515.1:n.625-8C>A
XM_006724780.2:c.625-8C>A	XP_006724843.1:n.625-8C>A
XM_006724781.2:c.625-8C>A	XP_006724844.1:n.625-8C>A
XM_011531378.1:c.625-8C>A	XP_011529680.1:n.625-8C>A
XM_011531379.1:c.625-8C>A	XP_011529681.1:n.625-8C>A
XM_017029737.1:c.625-8C>A	XP_016885226.1:n.625-8C>A
XM_017029738.1:c.625-8C>A	XP_016885227.1:n.625-8C>A
XM_017029739.1:c.625-8C>A	XP_016885228.1:n.625-8C>A
XM_017029740.1:c.625-8C>A	XP_016885229.1:n.625-8C>A
NM_080632.3:c.625-8C>A MANE Select	NP_542199.1:n.625-8C>A
NM_023010.4:c.625-8C>A	NP_075386.1:n.625-8C>A