Canonical Allele Identifier: CA2575610198
Gene: UBR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218454C>A , CM000676.2:g.93218454C>A GRCh38
NC_000014.8:g.93684800C>A , CM000676.1:g.93684800C>A GRCh37
NC_000014.7:g.92754553C>A NCBI36
NG_051089.1:g.16399C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-73C>A MANE Select ENSP00000013070.6:n.602-73C>A
ENST00000013070.10:c.602-73C>A ENSP00000013070.6:n.602-73C>A
ENST00000416753.5:c.374-73C>A ENSP00000391706.2:n.374-73C>A
ENST00000553674.1:c.*303-73C>A ENSP00000450470.1:n.*303-73C>A
ENST00000553857.5:c.378+3173C>A
ENST00000554232.5:c.506-73C>A ENSP00000450645.1:n.506-73C>A
ENST00000556871.5:c.311-73C>A ENSP00000451022.1:n.311-73C>A
ENST00000557048.1:n.511-73C>A
NM_175748.3:c.602-73C>A NP_786924.2:n.602-73C>A
NR_038150.1:n.704-73C>A
NM_175748.4:c.602-73C>A MANE Select NP_786924.2:n.602-73C>A
NR_038150.2:n.504-73C>A