Canonical Allele Identifier: CA969166842
Gene: UBR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958167_42958168insTT , CM000677.2:g.42958167_42958168insTT GRCh38
NC_000015.9:g.43250365_43250366insTT , CM000677.1:g.43250365_43250366insTT GRCh37
NC_000015.8:g.41037657_41037658insTT NCBI36
NG_012182.1:g.152921_152922insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4758-78_4758-77insAA MANE Select ENSP00000290650.4:n.4758-78_4758-77insAA
ENST00000290650.8:c.4758-78_4758-77insAA ENSP00000290650.4:n.4758-78_4758-77insAA
NM_174916.2:c.4758-78_4758-77insAA NP_777576.1:n.4758-78_4758-77insAA
NM_174916.3:c.4758-78_4758-77insAA MANE Select NP_777576.1:n.4758-78_4758-77insAA