Canonical Allele Identifier: CA2155440947
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218402C= , CM000676.2:g.93218402C= GRCh38
NC_000014.8:g.93684748C= , CM000676.1:g.93684748C= GRCh37
NC_000014.7:g.92754501C= NCBI36
NG_051089.1:g.16347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-125C= MANE Select ENSP00000013070.6:n.602-125C=
ENST00000013070.10:c.602-125C= ENSP00000013070.6:n.602-125C=
ENST00000416753.5:c.374-125C= ENSP00000391706.2:n.374-125C=
ENST00000553674.1:c.*303-125C= ENSP00000450470.1:n.*303-125C=
ENST00000553857.5:c.378+3121C=
ENST00000554232.5:c.506-125C= ENSP00000450645.1:n.506-125C=
ENST00000556871.5:c.311-125C= ENSP00000451022.1:n.311-125C=
ENST00000557048.1:n.511-125C=
NM_175748.3:c.602-125C= NP_786924.2:n.602-125C=
NR_038150.1:n.704-125C=
NM_175748.4:c.602-125C= MANE Select NP_786924.2:n.602-125C=
NR_038150.2:n.504-125C=