Canonical Allele Identifier: CA144280
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065551del , CM000672.2:g.17065551del GRCh38
NC_000010.10:g.17107550del , CM000672.1:g.17107550del GRCh37
NC_000010.9:g.17147556del NCBI36
NG_008967.1:g.69267del , LRG_540:g.69267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3096del MANE Select ENSP00000367064.4:p.Tyr1032Ter
ENST00000377833.8:c.3096del ENSP00000367064.4:p.Tyr1032Ter
NM_001081.3:c.3096del , LRG_540t1:c.3096del NP_001072.2:p.Tyr1032Ter
XM_011519708.1:c.3096del XP_011518010.1:p.Tyr1032Ter
XM_011519708.2:c.3096del XP_011518010.1:p.Tyr1032Ter
NM_001081.4:c.3096del MANE Select NP_001072.2:p.Tyr1032Ter