Canonical Allele Identifier: CA2626239193

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218486-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218489_93218490del , CM000676.2:g.93218489_93218490del	GRCh38
NC_000014.8:g.93684835_93684836del , CM000676.1:g.93684835_93684836del	GRCh37
NC_000014.7:g.92754588_92754589del	NCBI36
NG_051089.1:g.16434_16435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-38_602-37del MANE Select	ENSP00000013070.6:n.602-38_602-37del
ENST00000013070.10:c.602-38_602-37del	ENSP00000013070.6:n.602-38_602-37del
ENST00000416753.5:c.374-38_374-37del	ENSP00000391706.2:n.374-38_374-37del
ENST00000553674.1:c.*303-38_*303-37del	ENSP00000450470.1:n.*303-38_*303-37del
ENST00000553857.5:c.378+3208_378+3209del
ENST00000554232.5:c.506-38_506-37del	ENSP00000450645.1:n.506-38_506-37del
ENST00000556871.5:c.311-38_311-37del	ENSP00000451022.1:n.311-38_311-37del
ENST00000557048.1:n.511-38_511-37del
NM_175748.3:c.602-38_602-37del	NP_786924.2:n.602-38_602-37del
NR_038150.1:n.704-38_704-37del
NM_175748.4:c.602-38_602-37del MANE Select	NP_786924.2:n.602-38_602-37del
NR_038150.2:n.504-38_504-37del