Canonical Allele Identifier: CA2155440961

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218422_93218424delinsAAT , CM000676.2:g.93218422_93218424delinsAAT	GRCh38
NC_000014.8:g.93684768_93684770delinsAAT , CM000676.1:g.93684768_93684770delinsAAT	GRCh37
NC_000014.7:g.92754521_92754523delinsAAT	NCBI36
NG_051089.1:g.16367_16369delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-105_602-103delinsAAT MANE Select	ENSP00000013070.6:n.602-105_602-103delinsAAT
ENST00000013070.10:c.602-105_602-103delinsAAT	ENSP00000013070.6:n.602-105_602-103delinsAAT
ENST00000416753.5:c.374-105_374-103delinsAAT	ENSP00000391706.2:n.374-105_374-103delinsAAT
ENST00000553674.1:c.*303-105_*303-103delinsAAT	ENSP00000450470.1:n.*303-105_*303-103delinsAAT
ENST00000553857.5:c.378+3141_378+3143delinsAAT
ENST00000554232.5:c.506-105_506-103delinsAAT	ENSP00000450645.1:n.506-105_506-103delinsAAT
ENST00000556871.5:c.311-105_311-103delinsAAT	ENSP00000451022.1:n.311-105_311-103delinsAAT
ENST00000557048.1:n.511-105_511-103delinsAAT
NM_175748.3:c.602-105_602-103delinsAAT	NP_786924.2:n.602-105_602-103delinsAAT
NR_038150.1:n.704-105_704-103delinsAAT
NM_175748.4:c.602-105_602-103delinsAAT MANE Select	NP_786924.2:n.602-105_602-103delinsAAT
NR_038150.2:n.504-105_504-103delinsAAT