Canonical Allele Identifier: CA2173020193
Gene: UBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43068028T= , CM000677.2:g.43068028T= GRCh38
NC_000015.9:g.43360226T= , CM000677.1:g.43360226T= GRCh37
NC_000015.8:g.41147518T= NCBI36
NG_012182.1:g.43061A=

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.668A= MANE Select ENSP00000290650.4:p.Asn223=
ENST00000290650.8:c.668A= ENSP00000290650.4:p.Asn223=
ENST00000546274.6:c.668A= ENSP00000477932.1:p.Asn223=
ENST00000563239.1:c.*202+2871A= ENSP00000456502.1:n.*202+2871A=
NM_174916.2:c.668A= NP_777576.1:p.Asn223=
NM_174916.3:c.668A= MANE Select NP_777576.1:p.Asn223=