Canonical Allele Identifier: CA2626239029

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218411-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218412_93218413insGA , CM000676.2:g.93218412_93218413insGA	GRCh38
NC_000014.8:g.93684758_93684759insGA , CM000676.1:g.93684758_93684759insGA	GRCh37
NC_000014.7:g.92754511_92754512insGA	NCBI36
NG_051089.1:g.16357_16358insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-115_602-114insGA MANE Select	ENSP00000013070.6:n.602-115_602-114insGA
ENST00000013070.10:c.602-115_602-114insGA	ENSP00000013070.6:n.602-115_602-114insGA
ENST00000416753.5:c.374-115_374-114insGA	ENSP00000391706.2:n.374-115_374-114insGA
ENST00000553674.1:c.*303-115_*303-114insGA	ENSP00000450470.1:n.*303-115_*303-114insGA
ENST00000553857.5:c.378+3131_378+3132insGA
ENST00000554232.5:c.506-115_506-114insGA	ENSP00000450645.1:n.506-115_506-114insGA
ENST00000556871.5:c.311-115_311-114insGA	ENSP00000451022.1:n.311-115_311-114insGA
ENST00000557048.1:n.511-115_511-114insGA
NM_175748.3:c.602-115_602-114insGA	NP_786924.2:n.602-115_602-114insGA
NR_038150.1:n.704-115_704-114insGA
NM_175748.4:c.602-115_602-114insGA MANE Select	NP_786924.2:n.602-115_602-114insGA
NR_038150.2:n.504-115_504-114insGA