Canonical Allele Identifier: CA2155440907

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218334_93218335delinsCT , CM000676.2:g.93218334_93218335delinsCT	GRCh38
NC_000014.8:g.93684680_93684681delinsCT , CM000676.1:g.93684680_93684681delinsCT	GRCh37
NC_000014.7:g.92754433_92754434delinsCT	NCBI36
NG_051089.1:g.16279_16280delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-193_602-192delinsCT MANE Select	ENSP00000013070.6:n.602-193_602-192delinsCT
ENST00000013070.10:c.602-193_602-192delinsCT	ENSP00000013070.6:n.602-193_602-192delinsCT
ENST00000416753.5:c.374-193_374-192delinsCT	ENSP00000391706.2:n.374-193_374-192delinsCT
ENST00000553674.1:c.*303-193_*303-192delinsCT	ENSP00000450470.1:n.*303-193_*303-192delinsCT
ENST00000553857.5:c.378+3053_378+3054delinsCT
ENST00000554232.5:c.506-193_506-192delinsCT	ENSP00000450645.1:n.506-193_506-192delinsCT
ENST00000556871.5:c.311-193_311-192delinsCT	ENSP00000451022.1:n.311-193_311-192delinsCT
ENST00000557048.1:n.511-193_511-192delinsCT
NM_175748.3:c.602-193_602-192delinsCT	NP_786924.2:n.602-193_602-192delinsCT
NR_038150.1:n.704-193_704-192delinsCT
NM_175748.4:c.602-193_602-192delinsCT MANE Select	NP_786924.2:n.602-193_602-192delinsCT
NR_038150.2:n.504-193_504-192delinsCT