Canonical Allele Identifier: CA2608396418
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-16828722-TAAAAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828731_16828735del , CM000672.2:g.16828731_16828735del GRCh38
NC_000010.10:g.16870730_16870734del , CM000672.1:g.16870730_16870734del GRCh37
NC_000010.9:g.16910736_16910740del NCBI36
NG_008967.1:g.306091_306095del , LRG_540:g.306091_306095del

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+78_10764+82del MANE Select ENSP00000367064.4:n.10764+78_10764+82del
ENST00000377833.8:c.10764+78_10764+82del ENSP00000367064.4:n.10764+78_10764+82del
NM_001081.3:c.10764+78_10764+82del , LRG_540t1:c.10764+78_10764+82del NP_001072.2:n.10764+78_10764+82del
XM_011519709.1:c.6750+78_6750+82del XP_011518011.1:n.6750+78_6750+82del
XM_011519710.1:c.6726+78_6726+82del XP_011518012.1:n.6726+78_6726+82del
XM_011519711.1:c.6606+78_6606+82del XP_011518013.1:n.6606+78_6606+82del
XM_011519709.2:c.6750+78_6750+82del XP_011518011.1:n.6750+78_6750+82del
XM_011519710.2:c.6726+78_6726+82del XP_011518012.1:n.6726+78_6726+82del
XM_011519711.3:c.6606+78_6606+82del XP_011518013.1:n.6606+78_6606+82del
NM_001081.4:c.10764+78_10764+82del MANE Select NP_001072.2:n.10764+78_10764+82del
Search 100 bp 5'
Search 100 bp 3'