Canonical Allele Identifier: CA966066916

Gene: UBR7

Linked Data

• dbSNP Id: rs1894633984
• gnomAD v3: 14-93218417-A-AT
• gnomAD v4: 14-93218417-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218417_93218418insT , CM000676.2:g.93218417_93218418insT	GRCh38
NC_000014.8:g.93684763_93684764insT , CM000676.1:g.93684763_93684764insT	GRCh37
NC_000014.7:g.92754516_92754517insT	NCBI36
NG_051089.1:g.16362_16363insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-110_602-109insT MANE Select	ENSP00000013070.6:n.602-110_602-109insT
ENST00000013070.10:c.602-110_602-109insT	ENSP00000013070.6:n.602-110_602-109insT
ENST00000416753.5:c.374-110_374-109insT	ENSP00000391706.2:n.374-110_374-109insT
ENST00000553674.1:c.*303-110_*303-109insT	ENSP00000450470.1:n.*303-110_*303-109insT
ENST00000553857.5:c.378+3136_378+3137insT
ENST00000554232.5:c.506-110_506-109insT	ENSP00000450645.1:n.506-110_506-109insT
ENST00000556871.5:c.311-110_311-109insT	ENSP00000451022.1:n.311-110_311-109insT
ENST00000557048.1:n.511-110_511-109insT
NM_175748.3:c.602-110_602-109insT	NP_786924.2:n.602-110_602-109insT
NR_038150.1:n.704-110_704-109insT
NM_175748.4:c.602-110_602-109insT MANE Select	NP_786924.2:n.602-110_602-109insT
NR_038150.2:n.504-110_504-109insT