Canonical Allele Identifier: CA2155441058
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218655G= , CM000676.2:g.93218655G= GRCh38
NC_000014.8:g.93685001G= , CM000676.1:g.93685001G= GRCh37
NC_000014.7:g.92754754G= NCBI36
NG_051089.1:g.16600G=

Transcript Alleles

HGVS Amino-acid change
ENST00000013070.11:c.730G= MANE Select ENSP00000013070.6:p.Gly244=
ENST00000013070.10:c.730G= ENSP00000013070.6:p.Gly244=
ENST00000416753.5:c.502G= ENSP00000391706.2:p.Gly168=
ENST00000553674.1:c.*431G= ENSP00000450470.1:n.*431G=
ENST00000553857.5:c.378+3374G=
ENST00000556871.5:c.439G= ENSP00000451022.1:p.Gly147=
NM_175748.3:c.730G= NP_786924.2:p.Gly244=
NR_038150.1:n.832G=
NM_175748.4:c.730G= MANE Select NP_786924.2:p.Gly244=
NR_038150.2:n.632G=