Canonical Allele Identifier: CA2155440963

Gene: UBR7

Linked Data

• dbSNP Id: rs1894634620
• gnomAD v4: 14-93218422-AATAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218424_93218428del , CM000676.2:g.93218424_93218428del	GRCh38
NC_000014.8:g.93684770_93684774del , CM000676.1:g.93684770_93684774del	GRCh37
NC_000014.7:g.92754523_92754527del	NCBI36
NG_051089.1:g.16369_16373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-103_602-99del MANE Select	ENSP00000013070.6:n.602-103_602-99del
ENST00000013070.10:c.602-103_602-99del	ENSP00000013070.6:n.602-103_602-99del
ENST00000416753.5:c.374-103_374-99del	ENSP00000391706.2:n.374-103_374-99del
ENST00000553674.1:c.*303-103_*303-99del	ENSP00000450470.1:n.*303-103_*303-99del
ENST00000553857.5:c.378+3143_378+3147del
ENST00000554232.5:c.506-103_506-99del	ENSP00000450645.1:n.506-103_506-99del
ENST00000556871.5:c.311-103_311-99del	ENSP00000451022.1:n.311-103_311-99del
ENST00000557048.1:n.511-103_511-99del
NM_175748.3:c.602-103_602-99del	NP_786924.2:n.602-103_602-99del
NR_038150.1:n.704-103_704-99del
NM_175748.4:c.602-103_602-99del MANE Select	NP_786924.2:n.602-103_602-99del
NR_038150.2:n.504-103_504-99del