Canonical Allele Identifier: CA2155441014
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218539C= , CM000676.2:g.93218539C= GRCh38
NC_000014.8:g.93684885C= , CM000676.1:g.93684885C= GRCh37
NC_000014.7:g.92754638C= NCBI36
NG_051089.1:g.16484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.614C= MANE Select ENSP00000013070.6:p.Ser205=
ENST00000013070.10:c.614C= ENSP00000013070.6:p.Ser205=
ENST00000416753.5:c.386C= ENSP00000391706.2:p.Ser129=
ENST00000553674.1:c.*315C= ENSP00000450470.1:n.*315C=
ENST00000553857.5:c.378+3258C=
ENST00000554232.5:c.518C= ENSP00000450645.1:p.Ser173=
ENST00000556871.5:c.323C= ENSP00000451022.1:p.Ser108=
ENST00000557048.1:n.523C=
NM_175748.3:c.614C= NP_786924.2:p.Ser205=
NR_038150.1:n.716C=
NM_175748.4:c.614C= MANE Select NP_786924.2:p.Ser205=
NR_038150.2:n.516C=