Canonical Allele Identifier: CA2173020190
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43068023T= , CM000677.2:g.43068023T= GRCh38
NC_000015.9:g.43360221T= , CM000677.1:g.43360221T= GRCh37
NC_000015.8:g.41147513T= NCBI36
NG_012182.1:g.43066A=

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.673A= MANE Select ENSP00000290650.4:p.Arg225=
ENST00000290650.8:c.673A= ENSP00000290650.4:p.Arg225=
ENST00000546274.6:c.673A= ENSP00000477932.1:p.Arg225=
ENST00000563239.1:c.*202+2876A= ENSP00000456502.1:n.*202+2876A=
NM_174916.2:c.673A= NP_777576.1:p.Arg225=
NM_174916.3:c.673A= MANE Select NP_777576.1:p.Arg225=