Canonical Allele Identifier: CA2155441003

Gene: UBR7

Linked Data

• dbSNP Id: rs1894637068
• gnomAD v4: 14-93218504-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218504T>G , CM000676.2:g.93218504T>G	GRCh38
NC_000014.8:g.93684850T>G , CM000676.1:g.93684850T>G	GRCh37
NC_000014.7:g.92754603T>G	NCBI36
NG_051089.1:g.16449T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-23T>G MANE Select	ENSP00000013070.6:n.602-23T>G
ENST00000013070.10:c.602-23T>G	ENSP00000013070.6:n.602-23T>G
ENST00000416753.5:c.374-23T>G	ENSP00000391706.2:n.374-23T>G
ENST00000553674.1:c.*303-23T>G	ENSP00000450470.1:n.*303-23T>G
ENST00000553857.5:c.378+3223T>G
ENST00000554232.5:c.506-23T>G	ENSP00000450645.1:n.506-23T>G
ENST00000556871.5:c.311-23T>G	ENSP00000451022.1:n.311-23T>G
ENST00000557048.1:n.511-23T>G
NM_175748.3:c.602-23T>G	NP_786924.2:n.602-23T>G
NR_038150.1:n.704-23T>G
NM_175748.4:c.602-23T>G MANE Select	NP_786924.2:n.602-23T>G
NR_038150.2:n.504-23T>G