Canonical Allele Identifier: CA2608396413
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-16828717-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828717C>T , CM000672.2:g.16828717C>T GRCh38
NC_000010.10:g.16870716C>T , CM000672.1:g.16870716C>T GRCh37
NC_000010.9:g.16910722C>T NCBI36
NG_008967.1:g.306101G>A , LRG_540:g.306101G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+88G>A MANE Select ENSP00000367064.4:n.10764+88G>A
ENST00000377833.8:c.10764+88G>A ENSP00000367064.4:n.10764+88G>A
NM_001081.3:c.10764+88G>A , LRG_540t1:c.10764+88G>A NP_001072.2:n.10764+88G>A
XM_011519709.1:c.6750+88G>A XP_011518011.1:n.6750+88G>A
XM_011519710.1:c.6726+88G>A XP_011518012.1:n.6726+88G>A
XM_011519711.1:c.6606+88G>A XP_011518013.1:n.6606+88G>A
XM_011519709.2:c.6750+88G>A XP_011518011.1:n.6750+88G>A
XM_011519710.2:c.6726+88G>A XP_011518012.1:n.6726+88G>A
XM_011519711.3:c.6606+88G>A XP_011518013.1:n.6606+88G>A
NM_001081.4:c.10764+88G>A MANE Select NP_001072.2:n.10764+88G>A
Search 100 bp 5'
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