Canonical Allele Identifier: CA925381803
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v3: 10-16828722-T-TAAAA
gnomAD v4: 10-16828722-T-TAAAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828732_16828735dup , CM000672.2:g.16828732_16828735dup GRCh38
NC_000010.10:g.16870731_16870734dup , CM000672.1:g.16870731_16870734dup GRCh37
NC_000010.9:g.16910737_16910740dup NCBI36
NG_008967.1:g.306092_306095dup , LRG_540:g.306092_306095dup

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+79_10764+82dup MANE Select ENSP00000367064.4:n.10764+79_10764+82dup
ENST00000377833.8:c.10764+79_10764+82dup ENSP00000367064.4:n.10764+79_10764+82dup
NM_001081.3:c.10764+79_10764+82dup , LRG_540t1:c.10764+79_10764+82dup NP_001072.2:n.10764+79_10764+82dup
XM_011519709.1:c.6750+79_6750+82dup XP_011518011.1:n.6750+79_6750+82dup
XM_011519710.1:c.6726+79_6726+82dup XP_011518012.1:n.6726+79_6726+82dup
XM_011519711.1:c.6606+79_6606+82dup XP_011518013.1:n.6606+79_6606+82dup
XM_011519709.2:c.6750+79_6750+82dup XP_011518011.1:n.6750+79_6750+82dup
XM_011519710.2:c.6726+79_6726+82dup XP_011518012.1:n.6726+79_6726+82dup
XM_011519711.3:c.6606+79_6606+82dup XP_011518013.1:n.6606+79_6606+82dup
NM_001081.4:c.10764+79_10764+82dup MANE Select NP_001072.2:n.10764+79_10764+82dup
Search 100 bp 5'
Search 100 bp 3'