Canonical Allele Identifier: CA376154279
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17107543A>T (hg19) chr10:g.17065544A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065544A>T , CM000672.2:g.17065544A>T GRCh38
NC_000010.10:g.17107543A>T , CM000672.1:g.17107543A>T GRCh37
NC_000010.9:g.17147549A>T NCBI36
NG_008967.1:g.69274T>A , LRG_540:g.69274T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.3103T>A MANE Select ENSP00000367064.4:p.Phe1035Ile
ENST00000377833.8:c.3103T>A ENSP00000367064.4:p.Phe1035Ile
NM_001081.3:c.3103T>A , LRG_540t1:c.3103T>A NP_001072.2:p.Phe1035Ile
XM_011519708.1:c.3103T>A XP_011518010.1:p.Phe1035Ile
XM_011519708.2:c.3103T>A XP_011518010.1:p.Phe1035Ile
NM_001081.4:c.3103T>A MANE Select NP_001072.2:p.Phe1035Ile
Search 100 bp 5'
Search 100 bp 3'