Canonical Allele Identifier: CA2626239060

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218421-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218421_93218422insG , CM000676.2:g.93218421_93218422insG	GRCh38
NC_000014.8:g.93684767_93684768insG , CM000676.1:g.93684767_93684768insG	GRCh37
NC_000014.7:g.92754520_92754521insG	NCBI36
NG_051089.1:g.16366_16367insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-106_602-105insG MANE Select	ENSP00000013070.6:n.602-106_602-105insG
ENST00000013070.10:c.602-106_602-105insG	ENSP00000013070.6:n.602-106_602-105insG
ENST00000416753.5:c.374-106_374-105insG	ENSP00000391706.2:n.374-106_374-105insG
ENST00000553674.1:c.*303-106_*303-105insG	ENSP00000450470.1:n.*303-106_*303-105insG
ENST00000553857.5:c.378+3140_378+3141insG
ENST00000554232.5:c.506-106_506-105insG	ENSP00000450645.1:n.506-106_506-105insG
ENST00000556871.5:c.311-106_311-105insG	ENSP00000451022.1:n.311-106_311-105insG
ENST00000557048.1:n.511-106_511-105insG
NM_175748.3:c.602-106_602-105insG	NP_786924.2:n.602-106_602-105insG
NR_038150.1:n.704-106_704-105insG
NM_175748.4:c.602-106_602-105insG MANE Select	NP_786924.2:n.602-106_602-105insG
NR_038150.2:n.504-106_504-105insG