Canonical Allele Identifier: CA2173015229
Gene: UBR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43048299T= , CM000677.2:g.43048299T= GRCh38
NC_000015.9:g.43340497T= , CM000677.1:g.43340497T= GRCh37
NC_000015.8:g.41127789T= NCBI36
NG_012182.1:g.62790A=

Transcript Alleles

HGVS Amino-acid change
ENST00000290650.9:c.1539+93A= MANE Select ENSP00000290650.4:n.1539+93A=
ENST00000290650.8:c.1539+93A= ENSP00000290650.4:n.1539+93A=
ENST00000546274.6:c.1539+93A= ENSP00000477932.1:n.1539+93A=
ENST00000563239.1:c.*203-1010A= ENSP00000456502.1:n.*203-1010A=
ENST00000569971.5:c.410+93A= ENSP00000455759.1:n.410+93A=
NM_174916.2:c.1539+93A= NP_777576.1:n.1539+93A=
NM_174916.3:c.1539+93A= MANE Select NP_777576.1:n.1539+93A=
Search 100 bp 5'
Search 100 bp 3'