Canonical Allele Identifier: CA2628084756
Gene: UBR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43048336_43048337insA , CM000677.2:g.43048336_43048337insA GRCh38
NC_000015.9:g.43340534_43340535insA , CM000677.1:g.43340534_43340535insA GRCh37
NC_000015.8:g.41127826_41127827insA NCBI36
NG_012182.1:g.62752_62753insT

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.1539+55_1539+56insT MANE Select ENSP00000290650.4:n.1539+55_1539+56insT
ENST00000290650.8:c.1539+55_1539+56insT ENSP00000290650.4:n.1539+55_1539+56insT
ENST00000546274.6:c.1539+55_1539+56insT ENSP00000477932.1:n.1539+55_1539+56insT
ENST00000563239.1:c.*203-1048_*203-1047insT ENSP00000456502.1:n.*203-1048_*203-1047in...
ENST00000569971.5:c.410+55_410+56insT ENSP00000455759.1:n.410+55_410+56insT
NM_174916.2:c.1539+55_1539+56insT NP_777576.1:n.1539+55_1539+56insT
NM_174916.3:c.1539+55_1539+56insT MANE Select NP_777576.1:n.1539+55_1539+56insT