Canonical Allele Identifier: CA1893309726
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824796_16824797delinsAG , CM000672.2:g.16824796_16824797delinsAG GRCh38
NC_000010.10:g.16866795_16866796delinsAG , CM000672.1:g.16866795_16866796delinsAG GRCh37
NC_000010.9:g.16906801_16906802delinsAG NCBI36
NG_008967.1:g.310021_310022delinsCT , LRG_540:g.310021_310022delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*178_*179delinsCT MANE Select ENSP00000367064.4:n.*178_*179delinsCT
ENST00000377833.8:c.*178_*179delinsCT ENSP00000367064.4:n.*178_*179delinsCT
NM_001081.3:c.*178_*179delinsCT , LRG_540t1:c.*178_*179delinsCT NP_001072.2:n.*178_*179delinsCT
XM_011519709.1:c.*178_*179delinsCT XP_011518011.1:n.*178_*179delinsCT
XM_011519710.1:c.*178_*179delinsCT XP_011518012.1:n.*178_*179delinsCT
XM_011519711.1:c.*178_*179delinsCT XP_011518013.1:n.*178_*179delinsCT
XM_011519709.2:c.*178_*179delinsCT XP_011518011.1:n.*178_*179delinsCT
XM_011519710.2:c.*178_*179delinsCT XP_011518012.1:n.*178_*179delinsCT
XM_011519711.3:c.*178_*179delinsCT XP_011518013.1:n.*178_*179delinsCT
NM_001081.4:c.*178_*179delinsCT MANE Select NP_001072.2:n.*178_*179delinsCT