Canonical Allele Identifier: CA2802634120
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218459_93218462del , CM000676.2:g.93218459_93218462del GRCh38
NC_000014.8:g.93684805_93684808del , CM000676.1:g.93684805_93684808del GRCh37
NC_000014.7:g.92754558_92754561del NCBI36
NG_051089.1:g.16404_16407del

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-68_602-65del MANE Select ENSP00000013070.6:n.602-68_602-65del
ENST00000013070.10:c.602-68_602-65del ENSP00000013070.6:n.602-68_602-65del
ENST00000416753.5:c.374-68_374-65del ENSP00000391706.2:n.374-68_374-65del
ENST00000553674.1:c.*303-68_*303-65del ENSP00000450470.1:n.*303-68_*303-65del
ENST00000553857.5:c.378+3178_378+3181del
ENST00000554232.5:c.506-68_506-65del ENSP00000450645.1:n.506-68_506-65del
ENST00000556871.5:c.311-68_311-65del ENSP00000451022.1:n.311-68_311-65del
ENST00000557048.1:n.511-68_511-65del
NM_175748.3:c.602-68_602-65del NP_786924.2:n.602-68_602-65del
NR_038150.1:n.704-68_704-65del
NM_175748.4:c.602-68_602-65del MANE Select NP_786924.2:n.602-68_602-65del
NR_038150.2:n.504-68_504-65del