Canonical Allele Identifier: CA2626238910

Gene: UBR7

Linked Data

• gnomAD v4: 14-93218381-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218381A>C , CM000676.2:g.93218381A>C	GRCh38
NC_000014.8:g.93684727A>C , CM000676.1:g.93684727A>C	GRCh37
NC_000014.7:g.92754480A>C	NCBI36
NG_051089.1:g.16326A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-146A>C MANE Select	ENSP00000013070.6:n.602-146A>C
ENST00000013070.10:c.602-146A>C	ENSP00000013070.6:n.602-146A>C
ENST00000416753.5:c.374-146A>C	ENSP00000391706.2:n.374-146A>C
ENST00000553674.1:c.*303-146A>C	ENSP00000450470.1:n.*303-146A>C
ENST00000553857.5:c.378+3100A>C
ENST00000554232.5:c.506-146A>C	ENSP00000450645.1:n.506-146A>C
ENST00000556871.5:c.311-146A>C	ENSP00000451022.1:n.311-146A>C
ENST00000557048.1:n.511-146A>C
NM_175748.3:c.602-146A>C	NP_786924.2:n.602-146A>C
NR_038150.1:n.704-146A>C
NM_175748.4:c.602-146A>C MANE Select	NP_786924.2:n.602-146A>C
NR_038150.2:n.504-146A>C