Canonical Allele Identifier: CA2608400613
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065415G>A , CM000672.2:g.17065415G>A GRCh38
NC_000010.10:g.17107414G>A , CM000672.1:g.17107414G>A GRCh37
NC_000010.9:g.17147420G>A NCBI36
NG_008967.1:g.69403C>T , LRG_540:g.69403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3139+93C>T MANE Select ENSP00000367064.4:n.3139+93C>T
ENST00000377833.8:c.3139+93C>T ENSP00000367064.4:n.3139+93C>T
NM_001081.3:c.3139+93C>T , LRG_540t1:c.3139+93C>T NP_001072.2:n.3139+93C>T
XM_011519708.1:c.3139+93C>T XP_011518010.1:n.3139+93C>T
XM_011519708.2:c.3139+93C>T XP_011518010.1:n.3139+93C>T
NM_001081.4:c.3139+93C>T MANE Select NP_001072.2:n.3139+93C>T