Canonical Allele Identifier: CA2172970249
Gene: UBR1 HGNC NCBI

Linked Data

dbSNP Id: rs1694736981

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958292_42958302del , CM000677.2:g.42958292_42958302del GRCh38
NC_000015.9:g.43250490_43250500del , CM000677.1:g.43250490_43250500del GRCh37
NC_000015.8:g.41037782_41037792del NCBI36
NG_012182.1:g.152787_152797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-212_4758-202del MANE Select ENSP00000290650.4:n.4758-212_4758-202del
ENST00000290650.8:c.4758-212_4758-202del ENSP00000290650.4:n.4758-212_4758-202del
NM_174916.2:c.4758-212_4758-202del NP_777576.1:n.4758-212_4758-202del
NM_174916.3:c.4758-212_4758-202del MANE Select NP_777576.1:n.4758-212_4758-202del