Canonical Allele Identifier: CA390810708

Gene: UBR7

Linked Data

• COSMIC: COSM5848744
• MyVariant Identifiers: chr14:g.93684899G>A (hg19) ; chr14:g.93218553G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218553G>A , CM000676.2:g.93218553G>A	GRCh38
NC_000014.8:g.93684899G>A , CM000676.1:g.93684899G>A	GRCh37
NC_000014.7:g.92754652G>A	NCBI36
NG_051089.1:g.16498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.628G>A MANE Select	ENSP00000013070.6:p.Gly210Arg
ENST00000013070.10:c.628G>A	ENSP00000013070.6:p.Gly210Arg
ENST00000416753.5:c.400G>A	ENSP00000391706.2:p.Gly134Arg
ENST00000553674.1:c.*329G>A	ENSP00000450470.1:n.*329G>A
ENST00000553857.5:c.378+3272G>A
ENST00000554232.5:c.532G>A	ENSP00000450645.1:p.Gly178Arg
ENST00000556871.5:c.337G>A	ENSP00000451022.1:p.Gly113Arg
ENST00000557048.1:n.537G>A
NM_175748.3:c.628G>A	NP_786924.2:p.Gly210Arg
NR_038150.1:n.730G>A
NM_175748.4:c.628G>A MANE Select	NP_786924.2:p.Gly210Arg
NR_038150.2:n.530G>A