Canonical Allele Identifier: CA2155440976

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218454_93218458delinsCTGTT , CM000676.2:g.93218454_93218458delinsCTGTT	GRCh38
NC_000014.8:g.93684800_93684804delinsCTGTT , CM000676.1:g.93684800_93684804delinsCTGTT	GRCh37
NC_000014.7:g.92754553_92754557delinsCTGTT	NCBI36
NG_051089.1:g.16399_16403delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-73_602-69delinsCTGTT MANE Select	ENSP00000013070.6:n.602-73_602-69delinsCTGTT
ENST00000013070.10:c.602-73_602-69delinsCTGTT	ENSP00000013070.6:n.602-73_602-69delinsCTGTT
ENST00000416753.5:c.374-73_374-69delinsCTGTT	ENSP00000391706.2:n.374-73_374-69delinsCTGTT
ENST00000553674.1:c.*303-73_*303-69delinsCTGTT	ENSP00000450470.1:n.*303-73_*303-69delinsCTGTT
ENST00000553857.5:c.378+3173_378+3177delinsCTGTT
ENST00000554232.5:c.506-73_506-69delinsCTGTT	ENSP00000450645.1:n.506-73_506-69delinsCTGTT
ENST00000556871.5:c.311-73_311-69delinsCTGTT	ENSP00000451022.1:n.311-73_311-69delinsCTGTT
ENST00000557048.1:n.511-73_511-69delinsCTGTT
NM_175748.3:c.602-73_602-69delinsCTGTT	NP_786924.2:n.602-73_602-69delinsCTGTT
NR_038150.1:n.704-73_704-69delinsCTGTT
NM_175748.4:c.602-73_602-69delinsCTGTT MANE Select	NP_786924.2:n.602-73_602-69delinsCTGTT
NR_038150.2:n.504-73_504-69delinsCTGTT