Canonical Allele Identifier: CA2155440945

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218401_93218403delinsACT , CM000676.2:g.93218401_93218403delinsACT	GRCh38
NC_000014.8:g.93684747_93684749delinsACT , CM000676.1:g.93684747_93684749delinsACT	GRCh37
NC_000014.7:g.92754500_92754502delinsACT	NCBI36
NG_051089.1:g.16346_16348delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-126_602-124delinsACT MANE Select	ENSP00000013070.6:n.602-126_602-124delinsACT
ENST00000013070.10:c.602-126_602-124delinsACT	ENSP00000013070.6:n.602-126_602-124delinsACT
ENST00000416753.5:c.374-126_374-124delinsACT	ENSP00000391706.2:n.374-126_374-124delinsACT
ENST00000553674.1:c.*303-126_*303-124delinsACT	ENSP00000450470.1:n.*303-126_*303-124delinsACT
ENST00000553857.5:c.378+3120_378+3122delinsACT
ENST00000554232.5:c.506-126_506-124delinsACT	ENSP00000450645.1:n.506-126_506-124delinsACT
ENST00000556871.5:c.311-126_311-124delinsACT	ENSP00000451022.1:n.311-126_311-124delinsACT
ENST00000557048.1:n.511-126_511-124delinsACT
NM_175748.3:c.602-126_602-124delinsACT	NP_786924.2:n.602-126_602-124delinsACT
NR_038150.1:n.704-126_704-124delinsACT
NM_175748.4:c.602-126_602-124delinsACT MANE Select	NP_786924.2:n.602-126_602-124delinsACT
NR_038150.2:n.504-126_504-124delinsACT