Canonical Allele Identifier: CA490120002
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43340626A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43048428A>T , CM000677.2:g.43048428A>T GRCh38
NC_000015.9:g.43340626A>T , CM000677.1:g.43340626A>T GRCh37
NC_000015.8:g.41127918A>T NCBI36
NG_012182.1:g.62661T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.1503T>A MANE Select ENSP00000290650.4:p.Gly501=
ENST00000290650.8:c.1503T>A ENSP00000290650.4:p.Gly501=
ENST00000546274.6:c.1503T>A ENSP00000477932.1:p.Gly501=
ENST00000563239.1:c.*203-1139T>A ENSP00000456502.1:n.*203-1139T>A
ENST00000569971.5:c.374T>A ENSP00000455759.1:n.374T>A
NM_174916.2:c.1503T>A NP_777576.1:p.Gly501=
NM_174916.3:c.1503T>A MANE Select NP_777576.1:p.Gly501=
Search 100 bp 5'
Search 100 bp 3'