Canonical Allele Identifier: CA2155440941

Gene: UBR7

Linked Data

• dbSNP Id: rs1894633198
• gnomAD v4: 14-93218393-AGAGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218397_93218400del , CM000676.2:g.93218397_93218400del	GRCh38
NC_000014.8:g.93684743_93684746del , CM000676.1:g.93684743_93684746del	GRCh37
NC_000014.7:g.92754496_92754499del	NCBI36
NG_051089.1:g.16342_16345del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-130_602-127del MANE Select	ENSP00000013070.6:n.602-130_602-127del
ENST00000013070.10:c.602-130_602-127del	ENSP00000013070.6:n.602-130_602-127del
ENST00000416753.5:c.374-130_374-127del	ENSP00000391706.2:n.374-130_374-127del
ENST00000553674.1:c.*303-130_*303-127del	ENSP00000450470.1:n.*303-130_*303-127del
ENST00000553857.5:c.378+3116_378+3119del
ENST00000554232.5:c.506-130_506-127del	ENSP00000450645.1:n.506-130_506-127del
ENST00000556871.5:c.311-130_311-127del	ENSP00000451022.1:n.311-130_311-127del
ENST00000557048.1:n.511-130_511-127del
NM_175748.3:c.602-130_602-127del	NP_786924.2:n.602-130_602-127del
NR_038150.1:n.704-130_704-127del
NM_175748.4:c.602-130_602-127del MANE Select	NP_786924.2:n.602-130_602-127del
NR_038150.2:n.504-130_504-127del