Canonical Allele Identifier: CA376119766
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828818G>T , CM000672.2:g.16828818G>T GRCh38
NC_000010.10:g.16870817G>T , CM000672.1:g.16870817G>T GRCh37
NC_000010.9:g.16910823G>T NCBI36
NG_008967.1:g.306000C>A , LRG_540:g.306000C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10751C>A MANE Select ENSP00000367064.4:p.Pro3584Gln
ENST00000377833.8:c.10751C>A ENSP00000367064.4:p.Pro3584Gln
NM_001081.3:c.10751C>A , LRG_540t1:c.10751C>A NP_001072.2:p.Pro3584Gln
XM_011519709.1:c.6737C>A XP_011518011.1:p.Pro2246Gln
XM_011519710.1:c.6713C>A XP_011518012.1:p.Pro2238Gln
XM_011519711.1:c.6593C>A XP_011518013.1:p.Pro2198Gln
XM_011519709.2:c.6737C>A XP_011518011.1:p.Pro2246Gln
XM_011519710.2:c.6713C>A XP_011518012.1:p.Pro2238Gln
XM_011519711.3:c.6593C>A XP_011518013.1:p.Pro2198Gln
NM_001081.4:c.10751C>A MANE Select NP_001072.2:p.Pro3584Gln