Canonical Allele Identifier: CA392070093
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43340619A>C (hg19) chr15:g.43048421A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43048421A>C , CM000677.2:g.43048421A>C GRCh38
NC_000015.9:g.43340619A>C , CM000677.1:g.43340619A>C GRCh37
NC_000015.8:g.41127911A>C NCBI36
NG_012182.1:g.62668T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.1510T>G MANE Select ENSP00000290650.4:p.Ser504Ala
ENST00000290650.8:c.1510T>G ENSP00000290650.4:p.Ser504Ala
ENST00000546274.6:c.1510T>G ENSP00000477932.1:p.Ser504Ala
ENST00000563239.1:c.*203-1132T>G ENSP00000456502.1:n.*203-1132T>G
ENST00000569971.5:c.381T>G ENSP00000455759.1:n.381T>G
NM_174916.2:c.1510T>G NP_777576.1:p.Ser504Ala
NM_174916.3:c.1510T>G MANE Select NP_777576.1:p.Ser504Ala
Search 100 bp 5'
Search 100 bp 3'