Canonical Allele Identifier: CA2172970220
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958251C= , CM000677.2:g.42958251C= GRCh38
NC_000015.9:g.43250449C= , CM000677.1:g.43250449C= GRCh37
NC_000015.8:g.41037741C= NCBI36
NG_012182.1:g.152838G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-161G= MANE Select ENSP00000290650.4:n.4758-161G=
ENST00000290650.8:c.4758-161G= ENSP00000290650.4:n.4758-161G=
NM_174916.2:c.4758-161G= NP_777576.1:n.4758-161G=
NM_174916.3:c.4758-161G= MANE Select NP_777576.1:n.4758-161G=