Canonical Allele Identifier: CA2155441059
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218656G= , CM000676.2:g.93218656G= GRCh38
NC_000014.8:g.93685002G= , CM000676.1:g.93685002G= GRCh37
NC_000014.7:g.92754755G= NCBI36
NG_051089.1:g.16601G=

Transcript Alleles

HGVS Amino-acid change
ENST00000013070.11:c.731G= MANE Select ENSP00000013070.6:p.Gly244=
ENST00000013070.10:c.731G= ENSP00000013070.6:p.Gly244=
ENST00000416753.5:c.503G= ENSP00000391706.2:p.Gly168=
ENST00000553674.1:c.*432G= ENSP00000450470.1:n.*432G=
ENST00000553857.5:c.378+3375G=
ENST00000556871.5:c.440G= ENSP00000451022.1:p.Gly147=
NM_175748.3:c.731G= NP_786924.2:p.Gly244=
NR_038150.1:n.833G=
NM_175748.4:c.731G= MANE Select NP_786924.2:p.Gly244=
NR_038150.2:n.633G=