Canonical Allele Identifier: CA203531179
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 877209
ClinVar RCV Id: RCV001102739
dbSNP Id: rs529415832
gnomAD v2: 10-16866676-C-T
gnomAD v3: 10-16824677-C-T
gnomAD v4: 10-16824677-C-T
MyVariant Identifiers: chr10:g.16866676C>T (hg19) chr10:g.16824677C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824677C>T , CM000672.2:g.16824677C>T GRCh38
NC_000010.10:g.16866676C>T , CM000672.1:g.16866676C>T GRCh37
NC_000010.9:g.16906682C>T NCBI36
NG_008967.1:g.310141G>A , LRG_540:g.310141G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*298G>A MANE Select ENSP00000367064.4:n.*298G>A
ENST00000377833.8:c.*298G>A ENSP00000367064.4:n.*298G>A
NM_001081.3:c.*298G>A , LRG_540t1:c.*298G>A NP_001072.2:n.*298G>A
XM_011519709.1:c.*298G>A XP_011518011.1:n.*298G>A
XM_011519710.1:c.*298G>A XP_011518012.1:n.*298G>A
XM_011519711.1:c.*298G>A XP_011518013.1:n.*298G>A
XM_011519709.2:c.*298G>A XP_011518011.1:n.*298G>A
XM_011519710.2:c.*298G>A XP_011518012.1:n.*298G>A
XM_011519711.3:c.*298G>A XP_011518013.1:n.*298G>A
NM_001081.4:c.*298G>A MANE Select NP_001072.2:n.*298G>A
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