Canonical Allele Identifier: CA5425704
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 299545
dbSNP Id: rs375431948

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17126808A>G , CM000672.2:g.17126808A>G GRCh38
NC_000010.10:g.17168807A>G , CM000672.1:g.17168807A>G GRCh37
NC_000010.9:g.17208813A>G NCBI36
NG_008967.1:g.8010T>C , LRG_540:g.8010T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.349-9T>C MANE Select ENSP00000367064.4:p.=
ENST00000377823.1:c.349-9T>C ENSP00000367054.1:p.=
ENST00000377833.8:c.349-9T>C ENSP00000367064.4:p.=
ENST00000433666.5:n.10-9T>C ENSP00000415970.1:p.=
NM_001081.3:c.349-9T>C , LRG_540t1:c.349-9T>C NP_001072.2:p.=
XM_011519708.1:c.349-9T>C XP_011518010.1:p.=
XM_011519708.2:c.349-9T>C XP_011518010.1:p.=
NM_001081.4:c.349-9T>C MANE Select NP_001072.2:p.=