Canonical Allele Identifier: CA2224882235
Gene: USB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.58018969C= , CM000678.2:g.58018969C= GRCh38
NC_000016.9:g.58052873C= , CM000678.1:g.58052873C= GRCh37
NC_000016.8:g.56610374C= NCBI36
NG_027698.1:g.22597C= , LRG_352:g.22597C=

Transcript Alleles

HGVS Amino-acid change
ENST00000561568.6:c.571-3C= ENSP00000457322.2:n.571-3C=
ENST00000565662.6:c.*89-3C= ENSP00000513729.1:n.*89-3C=
ENST00000698444.1:c.457-3C= ENSP00000513726.1:n.457-3C=
ENST00000698445.1:c.504-3C= ENSP00000513727.1:n.504-3C=
ENST00000698446.1:c.*301-3C= ENSP00000513728.1:n.*301-3C=
ENST00000698447.1:c.*267-3C= ENSP00000513732.1:n.*267-3C=
ENST00000219281.8:c.610-3C= MANE Select ENSP00000219281.3:n.610-3C=
ENST00000219281.7:c.610-3C= ENSP00000219281.3:n.610-3C=
ENST00000539737.6:c.556-3C= ENSP00000446143.2:n.556-3C=
ENST00000561743.5:c.457-3C= ENSP00000454928.1:n.457-3C=
ENST00000565151.1:n.805-3C=
ENST00000565662.5:n.655-3C=
ENST00000566082.1:n.2328-3C=
NM_001195302.1:c.556-3C= NP_001182231.1:n.556-3C=
NM_024598.3:c.610-3C= , LRG_352t1:c.610-3C= NP_078874.2:n.610-3C=
XM_005256144.3:c.457-3C= XP_005256201.1:n.457-3C=
XM_011523328.1:c.571-3C= XP_011521630.1:n.571-3C=
XM_011523329.1:c.457-3C= XP_011521631.1:n.457-3C=
NM_001330568.1:c.457-3C= NP_001317497.1:n.457-3C=
NM_001195302.2:c.556-3C= NP_001182231.1:n.556-3C=
NM_001330568.2:c.457-3C= NP_001317497.1:n.457-3C=
NM_024598.4:c.610-3C= MANE Select NP_078874.2:n.610-3C=