Canonical Allele Identifier: CA2608396049
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824659del , CM000672.2:g.16824659del GRCh38
NC_000010.10:g.16866658del , CM000672.1:g.16866658del GRCh37
NC_000010.9:g.16906664del NCBI36
NG_008967.1:g.310160del , LRG_540:g.310160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*317del MANE Select ENSP00000367064.4:n.*317del
ENST00000377833.8:c.*317del ENSP00000367064.4:n.*317del
NM_001081.3:c.*317del , LRG_540t1:c.*317del NP_001072.2:n.*317del
XM_011519709.1:c.*317del XP_011518011.1:n.*317del
XM_011519710.1:c.*317del XP_011518012.1:n.*317del
XM_011519711.1:c.*317del XP_011518013.1:n.*317del
XM_011519709.2:c.*317del XP_011518011.1:n.*317del
XM_011519710.2:c.*317del XP_011518012.1:n.*317del
XM_011519711.3:c.*317del XP_011518013.1:n.*317del
NM_001081.4:c.*317del MANE Select NP_001072.2:n.*317del