Canonical Allele Identifier: CA392057967
Gene: UBR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43250249A>T (hg19) chr15:g.42958051A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42958051A>T , CM000677.2:g.42958051A>T GRCh38
NC_000015.9:g.43250249A>T , CM000677.1:g.43250249A>T GRCh37
NC_000015.8:g.41037541A>T NCBI36
NG_012182.1:g.153038T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290650.9:c.4797T>A MANE Select ENSP00000290650.4:p.Asp1599Glu
ENST00000290650.8:c.4797T>A ENSP00000290650.4:p.Asp1599Glu
NM_174916.2:c.4797T>A NP_777576.1:p.Asp1599Glu
NM_174916.3:c.4797T>A MANE Select NP_777576.1:p.Asp1599Glu
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Search 100 bp 3'