Canonical Allele Identifier: CA203533444
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs370322118
gnomAD v2: 10-16870721-TAAAAAA-T
gnomAD v3: 10-16828722-TAAAAAA-T
gnomAD v4: 10-16828722-TAAAAAA-T
MyVariant Identifiers: chr10:g.16870722_16870727del (hg19) chr10:g.16828723_16828728del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828730_16828735del , CM000672.2:g.16828730_16828735del GRCh38
NC_000010.10:g.16870729_16870734del , CM000672.1:g.16870729_16870734del GRCh37
NC_000010.9:g.16910735_16910740del NCBI36
NG_008967.1:g.306090_306095del , LRG_540:g.306090_306095del

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+77_10764+82del MANE Select ENSP00000367064.4:n.10764+77_10764+82del
ENST00000377833.8:c.10764+77_10764+82del ENSP00000367064.4:n.10764+77_10764+82del
NM_001081.3:c.10764+77_10764+82del , LRG_540t1:c.10764+77_10764+82del NP_001072.2:n.10764+77_10764+82del
XM_011519709.1:c.6750+77_6750+82del XP_011518011.1:n.6750+77_6750+82del
XM_011519710.1:c.6726+77_6726+82del XP_011518012.1:n.6726+77_6726+82del
XM_011519711.1:c.6606+77_6606+82del XP_011518013.1:n.6606+77_6606+82del
XM_011519709.2:c.6750+77_6750+82del XP_011518011.1:n.6750+77_6750+82del
XM_011519710.2:c.6726+77_6726+82del XP_011518012.1:n.6726+77_6726+82del
XM_011519711.3:c.6606+77_6606+82del XP_011518013.1:n.6606+77_6606+82del
NM_001081.4:c.10764+77_10764+82del MANE Select NP_001072.2:n.10764+77_10764+82del
Search 100 bp 5'
Search 100 bp 3'