Canonical Allele Identifier: CA489907284
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43250282A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958084A>T , CM000677.2:g.42958084A>T GRCh38
NC_000015.9:g.43250282A>T , CM000677.1:g.43250282A>T GRCh37
NC_000015.8:g.41037574A>T NCBI36
NG_012182.1:g.153005T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4764T>A MANE Select ENSP00000290650.4:p.Pro1588=
ENST00000290650.8:c.4764T>A ENSP00000290650.4:p.Pro1588=
NM_174916.2:c.4764T>A NP_777576.1:p.Pro1588=
NM_174916.3:c.4764T>A MANE Select NP_777576.1:p.Pro1588=