Canonical Allele Identifier: CA144302
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 56342
ClinVar RCV Id: RCV000049755
dbSNP Id: rs386833790
MyVariant Identifiers: chr10:g.17157517A>T (hg19) chr10:g.17115518A>T (hg38)
PubMed: PMID:22929189
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17115518A>T , CM000672.2:g.17115518A>T GRCh38
NC_000010.10:g.17157517A>T , CM000672.1:g.17157517A>T GRCh37
NC_000010.9:g.17197523A>T NCBI36
NG_008967.1:g.19300T>A , LRG_540:g.19300T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.673T>A MANE Select ENSP00000367064.4:p.Cys225Ser
ENST00000377833.8:c.673T>A ENSP00000367064.4:p.Cys225Ser
NM_001081.3:c.673T>A , LRG_540t1:c.673T>A NP_001072.2:p.Cys225Ser
XM_011519708.1:c.673T>A XP_011518010.1:p.Cys225Ser
XM_011519708.2:c.673T>A XP_011518010.1:p.Cys225Ser
NM_001081.4:c.673T>A MANE Select NP_001072.2:p.Cys225Ser
Search 100 bp 5'
Search 100 bp 3'