Canonical Allele Identifier: CA1177553187

Gene: USP33

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77757213T= , CM000663.2:g.77757213T=	GRCh38
NC_000001.10:g.78222898T= , CM000663.1:g.78222898T=	GRCh37
NC_000001.9:g.77995486T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370792.7:c.-138+2430A=	ENSP00000359828.3:n.-138+2430A=
ENST00000370793.5:c.-138+2430A=	ENSP00000359829.1:n.-138+2430A=
ENST00000370794.7:c.-52+2430A= MANE Select	ENSP00000359830.3:n.-52+2430A=
ENST00000524536.5:c.-296+2430A=	ENSP00000434441.1:n.-296+2430A=
ENST00000524778.1:c.-52+2488A=	ENSP00000436441.1:n.-52+2488A=
ENST00000525113.5:n.146+2488A=
ENST00000528150.1:n.169+2430A=
ENST00000530709.5:c.-177+2135A=	ENSP00000433283.1:n.-177+2135A=
NM_015017.4:c.-138+2430A=	NP_055832.3:n.-138+2430A=
NM_201624.2:c.-52+2430A=	NP_963918.1:n.-52+2430A=
NM_201626.2:c.-138+2430A=	NP_963920.1:n.-138+2430A=
XM_017000722.2:c.-52+2430A=	XP_016856211.1:n.-52+2430A=
XM_017000723.2:c.-52+2430A=	XP_016856212.1:n.-52+2430A=
XM_017000724.2:c.-52+2430A=	XP_016856213.1:n.-52+2430A=
XM_017000725.2:c.-52+2430A=	XP_016856214.1:n.-52+2430A=
XM_017000726.2:c.-52+2430A=	XP_016856215.1:n.-52+2430A=
XM_017000727.2:c.-548+2430A=	XP_016856216.1:n.-548+2430A=
NM_001377430.1:c.-138+2430A=	NP_001364359.1:n.-138+2430A=
NM_001377431.1:c.-52+2430A=	NP_001364360.1:n.-52+2430A=
NM_001377432.1:c.-138+2430A=	NP_001364361.1:n.-138+2430A=
NM_001377433.1:c.-138+2430A=	NP_001364362.1:n.-138+2430A=
NM_001377434.1:c.-52+2430A=	NP_001364363.1:n.-52+2430A=
NM_001377435.1:c.-52+2430A=	NP_001364364.1:n.-52+2430A=
NM_001377436.1:c.-52+2430A=	NP_001364365.1:n.-52+2430A=
NM_001377437.1:c.-52+2430A=	NP_001364366.1:n.-52+2430A=
NM_001377438.1:c.-548+2430A=	NP_001364367.1:n.-548+2430A=
NM_001377439.1:c.-727+2430A=	NP_001364368.1:n.-727+2430A=
NM_015017.5:c.-138+2430A=	NP_055832.3:n.-138+2430A=
NM_201624.3:c.-52+2430A= MANE Select	NP_963918.1:n.-52+2430A=
NM_201626.3:c.-138+2430A=	NP_963920.1:n.-138+2430A=