Canonical Allele Identifier: CA2155441033
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218575G= , CM000676.2:g.93218575G= GRCh38
NC_000014.8:g.93684921G= , CM000676.1:g.93684921G= GRCh37
NC_000014.7:g.92754674G= NCBI36
NG_051089.1:g.16520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.650G= MANE Select ENSP00000013070.6:p.Gly217=
ENST00000013070.10:c.650G= ENSP00000013070.6:p.Gly217=
ENST00000416753.5:c.422G= ENSP00000391706.2:p.Gly141=
ENST00000553674.1:c.*351G= ENSP00000450470.1:n.*351G=
ENST00000553857.5:c.378+3294G=
ENST00000556871.5:c.359G= ENSP00000451022.1:p.Gly120=
ENST00000557048.1:n.559G=
NM_175748.3:c.650G= NP_786924.2:p.Gly217=
NR_038150.1:n.752G=
NM_175748.4:c.650G= MANE Select NP_786924.2:p.Gly217=
NR_038150.2:n.552G=