Canonical Allele Identifier: CA2173015254
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43048361C= , CM000677.2:g.43048361C= GRCh38
NC_000015.9:g.43340559C= , CM000677.1:g.43340559C= GRCh37
NC_000015.8:g.41127851C= NCBI36
NG_012182.1:g.62728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.1539+31G= MANE Select ENSP00000290650.4:n.1539+31G=
ENST00000290650.8:c.1539+31G= ENSP00000290650.4:n.1539+31G=
ENST00000546274.6:c.1539+31G= ENSP00000477932.1:n.1539+31G=
ENST00000563239.1:c.*203-1072G= ENSP00000456502.1:n.*203-1072G=
ENST00000569971.5:c.410+31G= ENSP00000455759.1:n.410+31G=
NM_174916.2:c.1539+31G= NP_777576.1:n.1539+31G=
NM_174916.3:c.1539+31G= MANE Select NP_777576.1:n.1539+31G=