Canonical Allele Identifier: CA2608396179
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-16824824-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824827del , CM000672.2:g.16824827del GRCh38
NC_000010.10:g.16866826del , CM000672.1:g.16866826del GRCh37
NC_000010.9:g.16906832del NCBI36
NG_008967.1:g.309993del , LRG_540:g.309993del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*150del MANE Select ENSP00000367064.4:n.*150del
ENST00000377833.8:c.*150del ENSP00000367064.4:n.*150del
NM_001081.3:c.*150del , LRG_540t1:c.*150del NP_001072.2:n.*150del
XM_011519709.1:c.*150del XP_011518011.1:n.*150del
XM_011519710.1:c.*150del XP_011518012.1:n.*150del
XM_011519711.1:c.*150del XP_011518013.1:n.*150del
XM_011519709.2:c.*150del XP_011518011.1:n.*150del
XM_011519710.2:c.*150del XP_011518012.1:n.*150del
XM_011519711.3:c.*150del XP_011518013.1:n.*150del
NM_001081.4:c.*150del MANE Select NP_001072.2:n.*150del
Search 100 bp 5'
Search 100 bp 3'