Canonical Allele Identifier: CA2155440946

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218402_93218406delinsCTCTG , CM000676.2:g.93218402_93218406delinsCTCTG	GRCh38
NC_000014.8:g.93684748_93684752delinsCTCTG , CM000676.1:g.93684748_93684752delinsCTCTG	GRCh37
NC_000014.7:g.92754501_92754505delinsCTCTG	NCBI36
NG_051089.1:g.16347_16351delinsCTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-125_602-121delinsCTCTG MANE Select	ENSP00000013070.6:n.602-125_602-121delinsCTCTG
ENST00000013070.10:c.602-125_602-121delinsCTCTG	ENSP00000013070.6:n.602-125_602-121delinsCTCTG
ENST00000416753.5:c.374-125_374-121delinsCTCTG	ENSP00000391706.2:n.374-125_374-121delinsCTCTG
ENST00000553674.1:c.*303-125_*303-121delinsCTCTG	ENSP00000450470.1:n.*303-125_*303-121delinsCTCTG
ENST00000553857.5:c.378+3121_378+3125delinsCTCTG
ENST00000554232.5:c.506-125_506-121delinsCTCTG	ENSP00000450645.1:n.506-125_506-121delinsCTCTG
ENST00000556871.5:c.311-125_311-121delinsCTCTG	ENSP00000451022.1:n.311-125_311-121delinsCTCTG
ENST00000557048.1:n.511-125_511-121delinsCTCTG
NM_175748.3:c.602-125_602-121delinsCTCTG	NP_786924.2:n.602-125_602-121delinsCTCTG
NR_038150.1:n.704-125_704-121delinsCTCTG
NM_175748.4:c.602-125_602-121delinsCTCTG MANE Select	NP_786924.2:n.602-125_602-121delinsCTCTG
NR_038150.2:n.504-125_504-121delinsCTCTG