Canonical Allele Identifier: CA2155440964

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218423_93218424delinsAT , CM000676.2:g.93218423_93218424delinsAT	GRCh38
NC_000014.8:g.93684769_93684770delinsAT , CM000676.1:g.93684769_93684770delinsAT	GRCh37
NC_000014.7:g.92754522_92754523delinsAT	NCBI36
NG_051089.1:g.16368_16369delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-104_602-103delinsAT MANE Select	ENSP00000013070.6:n.602-104_602-103delinsAT
ENST00000013070.10:c.602-104_602-103delinsAT	ENSP00000013070.6:n.602-104_602-103delinsAT
ENST00000416753.5:c.374-104_374-103delinsAT	ENSP00000391706.2:n.374-104_374-103delinsAT
ENST00000553674.1:c.*303-104_*303-103delinsAT	ENSP00000450470.1:n.*303-104_*303-103delinsAT
ENST00000553857.5:c.378+3142_378+3143delinsAT
ENST00000554232.5:c.506-104_506-103delinsAT	ENSP00000450645.1:n.506-104_506-103delinsAT
ENST00000556871.5:c.311-104_311-103delinsAT	ENSP00000451022.1:n.311-104_311-103delinsAT
ENST00000557048.1:n.511-104_511-103delinsAT
NM_175748.3:c.602-104_602-103delinsAT	NP_786924.2:n.602-104_602-103delinsAT
NR_038150.1:n.704-104_704-103delinsAT
NM_175748.4:c.602-104_602-103delinsAT MANE Select	NP_786924.2:n.602-104_602-103delinsAT
NR_038150.2:n.504-104_504-103delinsAT