Canonical Allele Identifier: CA2626239064
Gene: UBR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218423_93218424insATAA , CM000676.2:g.93218423_93218424insATAA GRCh38
NC_000014.8:g.93684769_93684770insATAA , CM000676.1:g.93684769_93684770insATAA GRCh37
NC_000014.7:g.92754522_92754523insATAA NCBI36
NG_051089.1:g.16368_16369insATAA

Transcript Alleles

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