Canonical Allele Identifier: CA2626239048

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218419-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218419_93218420insT , CM000676.2:g.93218419_93218420insT	GRCh38
NC_000014.8:g.93684765_93684766insT , CM000676.1:g.93684765_93684766insT	GRCh37
NC_000014.7:g.92754518_92754519insT	NCBI36
NG_051089.1:g.16364_16365insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-108_602-107insT MANE Select	ENSP00000013070.6:n.602-108_602-107insT
ENST00000013070.10:c.602-108_602-107insT	ENSP00000013070.6:n.602-108_602-107insT
ENST00000416753.5:c.374-108_374-107insT	ENSP00000391706.2:n.374-108_374-107insT
ENST00000553674.1:c.*303-108_*303-107insT	ENSP00000450470.1:n.*303-108_*303-107insT
ENST00000553857.5:c.378+3138_378+3139insT
ENST00000554232.5:c.506-108_506-107insT	ENSP00000450645.1:n.506-108_506-107insT
ENST00000556871.5:c.311-108_311-107insT	ENSP00000451022.1:n.311-108_311-107insT
ENST00000557048.1:n.511-108_511-107insT
NM_175748.3:c.602-108_602-107insT	NP_786924.2:n.602-108_602-107insT
NR_038150.1:n.704-108_704-107insT
NM_175748.4:c.602-108_602-107insT MANE Select	NP_786924.2:n.602-108_602-107insT
NR_038150.2:n.504-108_504-107insT