Canonical Allele Identifier: CA390811306
Gene: UBR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218697G>C , CM000676.2:g.93218697G>C GRCh38
NC_000014.8:g.93685043G>C , CM000676.1:g.93685043G>C GRCh37
NC_000014.7:g.92754796G>C NCBI36
NG_051089.1:g.16642G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.772G>C MANE Select ENSP00000013070.6:p.Glu258Gln
ENST00000013070.10:c.772G>C ENSP00000013070.6:p.Glu258Gln
ENST00000416753.5:c.544G>C ENSP00000391706.2:p.Glu182Gln
ENST00000553674.1:c.*473G>C ENSP00000450470.1:n.*473G>C
ENST00000553857.5:c.378+3416G>C
ENST00000555329.1:c.17G>C
NM_175748.3:c.772G>C NP_786924.2:p.Glu258Gln
NR_038150.1:n.874G>C
NM_175748.4:c.772G>C MANE Select NP_786924.2:p.Glu258Gln
NR_038150.2:n.674G>C