Canonical Allele Identifier: CA2155441092
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218730C= , CM000676.2:g.93218730C= GRCh38
NC_000014.8:g.93685076C= , CM000676.1:g.93685076C= GRCh37
NC_000014.7:g.92754829C= NCBI36
NG_051089.1:g.16675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.805C= MANE Select ENSP00000013070.6:p.Leu269=
ENST00000013070.10:c.805C= ENSP00000013070.6:p.Leu269=
ENST00000416753.5:c.577C= ENSP00000391706.2:p.Leu193=
ENST00000553674.1:c.*506C= ENSP00000450470.1:n.*506C=
ENST00000553857.5:c.378+3449C=
ENST00000555329.1:c.50C=
NM_175748.3:c.805C= NP_786924.2:p.Leu269=
NR_038150.1:n.907C=
NM_175748.4:c.805C= MANE Select NP_786924.2:p.Leu269=
NR_038150.2:n.707C=