Canonical Allele Identifier: CA2155441080
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218703T= , CM000676.2:g.93218703T= GRCh38
NC_000014.8:g.93685049T= , CM000676.1:g.93685049T= GRCh37
NC_000014.7:g.92754802T= NCBI36
NG_051089.1:g.16648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.778T= MANE Select ENSP00000013070.6:p.Cys260=
ENST00000013070.10:c.778T= ENSP00000013070.6:p.Cys260=
ENST00000416753.5:c.550T= ENSP00000391706.2:p.Cys184=
ENST00000553674.1:c.*479T= ENSP00000450470.1:n.*479T=
ENST00000553857.5:c.378+3422T=
ENST00000555329.1:c.23T=
NM_175748.3:c.778T= NP_786924.2:p.Cys260=
NR_038150.1:n.880T=
NM_175748.4:c.778T= MANE Select NP_786924.2:p.Cys260=
NR_038150.2:n.680T=