Canonical Allele Identifier: CA2155440949
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218411_93218415delinsTAAAA , CM000676.2:g.93218411_93218415delinsTAAAA GRCh38
NC_000014.8:g.93684757_93684761delinsTAAAA , CM000676.1:g.93684757_93684761delinsTAAAA GRCh37
NC_000014.7:g.92754510_92754514delinsTAAAA NCBI36
NG_051089.1:g.16356_16360delinsTAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-116_602-112delinsTAAAA MANE Select ENSP00000013070.6:n.602-116_602-112delinsTAAAA
ENST00000013070.10:c.602-116_602-112delinsTAAAA ENSP00000013070.6:n.602-116_602-112delinsTAAAA
ENST00000416753.5:c.374-116_374-112delinsTAAAA ENSP00000391706.2:n.374-116_374-112delinsTAAAA
ENST00000553674.1:c.*303-116_*303-112delinsTAAAA ENSP00000450470.1:n.*303-116_*303-112delinsTAAAA
ENST00000553857.5:c.378+3130_378+3134delinsTAAAA
ENST00000554232.5:c.506-116_506-112delinsTAAAA ENSP00000450645.1:n.506-116_506-112delinsTAAAA
ENST00000556871.5:c.311-116_311-112delinsTAAAA ENSP00000451022.1:n.311-116_311-112delinsTAAAA
ENST00000557048.1:n.511-116_511-112delinsTAAAA
NM_175748.3:c.602-116_602-112delinsTAAAA NP_786924.2:n.602-116_602-112delinsTAAAA
NR_038150.1:n.704-116_704-112delinsTAAAA
NM_175748.4:c.602-116_602-112delinsTAAAA MANE Select NP_786924.2:n.602-116_602-112delinsTAAAA
NR_038150.2:n.504-116_504-112delinsTAAAA