Canonical Allele Identifier: CA2155441056
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218652C= , CM000676.2:g.93218652C= GRCh38
NC_000014.8:g.93684998C= , CM000676.1:g.93684998C= GRCh37
NC_000014.7:g.92754751C= NCBI36
NG_051089.1:g.16597C=

Transcript Alleles

HGVS Amino-acid change
ENST00000013070.11:c.727C= MANE Select ENSP00000013070.6:p.Gln243=
ENST00000013070.10:c.727C= ENSP00000013070.6:p.Gln243=
ENST00000416753.5:c.499C= ENSP00000391706.2:p.Gln167=
ENST00000553674.1:c.*428C= ENSP00000450470.1:n.*428C=
ENST00000553857.5:c.378+3371C=
ENST00000556871.5:c.436C= ENSP00000451022.1:p.Gln146=
NM_175748.3:c.727C= NP_786924.2:p.Gln243=
NR_038150.1:n.829C=
NM_175748.4:c.727C= MANE Select NP_786924.2:p.Gln243=
NR_038150.2:n.629C=