Canonical Allele Identifier: CA2608396142
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1838725048

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824802dup , CM000672.2:g.16824802dup GRCh38
NC_000010.10:g.16866801dup , CM000672.1:g.16866801dup GRCh37
NC_000010.9:g.16906807dup NCBI36
NG_008967.1:g.310021dup , LRG_540:g.310021dup

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*178dup MANE Select ENSP00000367064.4:n.*178dup
ENST00000377833.8:c.*178dup ENSP00000367064.4:n.*178dup
NM_001081.3:c.*178dup , LRG_540t1:c.*178dup NP_001072.2:n.*178dup
XM_011519709.1:c.*178dup XP_011518011.1:n.*178dup
XM_011519710.1:c.*178dup XP_011518012.1:n.*178dup
XM_011519711.1:c.*178dup XP_011518013.1:n.*178dup
XM_011519709.2:c.*178dup XP_011518011.1:n.*178dup
XM_011519710.2:c.*178dup XP_011518012.1:n.*178dup
XM_011519711.3:c.*178dup XP_011518013.1:n.*178dup
NM_001081.4:c.*178dup MANE Select NP_001072.2:n.*178dup