Canonical Allele Identifier: CA2802634114
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218368del , CM000676.2:g.93218368del GRCh38
NC_000014.8:g.93684714del , CM000676.1:g.93684714del GRCh37
NC_000014.7:g.92754467del NCBI36
NG_051089.1:g.16313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-159del MANE Select ENSP00000013070.6:n.602-159del
ENST00000013070.10:c.602-159del ENSP00000013070.6:n.602-159del
ENST00000416753.5:c.374-159del ENSP00000391706.2:n.374-159del
ENST00000553674.1:c.*303-159del ENSP00000450470.1:n.*303-159del
ENST00000553857.5:c.378+3087del
ENST00000554232.5:c.506-159del ENSP00000450645.1:n.506-159del
ENST00000556871.5:c.311-159del ENSP00000451022.1:n.311-159del
ENST00000557048.1:n.511-159del
NM_175748.3:c.602-159del NP_786924.2:n.602-159del
NR_038150.1:n.704-159del
NM_175748.4:c.602-159del MANE Select NP_786924.2:n.602-159del
NR_038150.2:n.504-159del