Canonical Allele Identifier: CA925381777
Gene: CUBN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828714_16828722del , CM000672.2:g.16828714_16828722del GRCh38
NC_000010.10:g.16870713_16870721del , CM000672.1:g.16870713_16870721del GRCh37
NC_000010.9:g.16910719_16910727del NCBI36
NG_008967.1:g.306096_306104del , LRG_540:g.306096_306104del

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+83_10764+91del MANE Select ENSP00000367064.4:n.10764+83_10764+91del
ENST00000377833.8:c.10764+83_10764+91del ENSP00000367064.4:n.10764+83_10764+91del
NM_001081.3:c.10764+83_10764+91del , LRG_540t1:c.10764+83_10764+91del NP_001072.2:n.10764+83_10764+91del
XM_011519709.1:c.6750+83_6750+91del XP_011518011.1:n.6750+83_6750+91del
XM_011519710.1:c.6726+83_6726+91del XP_011518012.1:n.6726+83_6726+91del
XM_011519711.1:c.6606+83_6606+91del XP_011518013.1:n.6606+83_6606+91del
XM_011519709.2:c.6750+83_6750+91del XP_011518011.1:n.6750+83_6750+91del
XM_011519710.2:c.6726+83_6726+91del XP_011518012.1:n.6726+83_6726+91del
XM_011519711.3:c.6606+83_6606+91del XP_011518013.1:n.6606+83_6606+91del
NM_001081.4:c.10764+83_10764+91del MANE Select NP_001072.2:n.10764+83_10764+91del
Search 100 bp 5'
Search 100 bp 3'