Canonical Allele Identifier: CA2626238956

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218397-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218400_93218401del , CM000676.2:g.93218400_93218401del	GRCh38
NC_000014.8:g.93684746_93684747del , CM000676.1:g.93684746_93684747del	GRCh37
NC_000014.7:g.92754499_92754500del	NCBI36
NG_051089.1:g.16345_16346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-127_602-126del MANE Select	ENSP00000013070.6:n.602-127_602-126del
ENST00000013070.10:c.602-127_602-126del	ENSP00000013070.6:n.602-127_602-126del
ENST00000416753.5:c.374-127_374-126del	ENSP00000391706.2:n.374-127_374-126del
ENST00000553674.1:c.*303-127_*303-126del	ENSP00000450470.1:n.*303-127_*303-126del
ENST00000553857.5:c.378+3119_378+3120del
ENST00000554232.5:c.506-127_506-126del	ENSP00000450645.1:n.506-127_506-126del
ENST00000556871.5:c.311-127_311-126del	ENSP00000451022.1:n.311-127_311-126del
ENST00000557048.1:n.511-127_511-126del
NM_175748.3:c.602-127_602-126del	NP_786924.2:n.602-127_602-126del
NR_038150.1:n.704-127_704-126del
NM_175748.4:c.602-127_602-126del MANE Select	NP_786924.2:n.602-127_602-126del
NR_038150.2:n.504-127_504-126del