Canonical Allele Identifier: CA2155441081
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218704G= , CM000676.2:g.93218704G= GRCh38
NC_000014.8:g.93685050G= , CM000676.1:g.93685050G= GRCh37
NC_000014.7:g.92754803G= NCBI36
NG_051089.1:g.16649G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.779G= MANE Select ENSP00000013070.6:p.Cys260=
ENST00000013070.10:c.779G= ENSP00000013070.6:p.Cys260=
ENST00000416753.5:c.551G= ENSP00000391706.2:p.Cys184=
ENST00000553674.1:c.*480G= ENSP00000450470.1:n.*480G=
ENST00000553857.5:c.378+3423G=
ENST00000555329.1:c.24G=
NM_175748.3:c.779G= NP_786924.2:p.Cys260=
NR_038150.1:n.881G=
NM_175748.4:c.779G= MANE Select NP_786924.2:p.Cys260=
NR_038150.2:n.681G=