Canonical Allele Identifier: CA592139950
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 878250
ClinVar RCV Id: RCV001104662
dbSNP Id: rs1203238498
gnomAD v2: 10-16866707-T-A
gnomAD v3: 10-16824708-T-A
gnomAD v4: 10-16824708-T-A
MyVariant Identifiers: chr10:g.16866707T>A (hg19) chr10:g.16824708T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824708T>A , CM000672.2:g.16824708T>A GRCh38
NC_000010.10:g.16866707T>A , CM000672.1:g.16866707T>A GRCh37
NC_000010.9:g.16906713T>A NCBI36
NG_008967.1:g.310110A>T , LRG_540:g.310110A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*267A>T MANE Select ENSP00000367064.4:n.*267A>T
ENST00000377833.8:c.*267A>T ENSP00000367064.4:n.*267A>T
NM_001081.3:c.*267A>T , LRG_540t1:c.*267A>T NP_001072.2:n.*267A>T
XM_011519709.1:c.*267A>T XP_011518011.1:n.*267A>T
XM_011519710.1:c.*267A>T XP_011518012.1:n.*267A>T
XM_011519711.1:c.*267A>T XP_011518013.1:n.*267A>T
XM_011519709.2:c.*267A>T XP_011518011.1:n.*267A>T
XM_011519710.2:c.*267A>T XP_011518012.1:n.*267A>T
XM_011519711.3:c.*267A>T XP_011518013.1:n.*267A>T
NM_001081.4:c.*267A>T MANE Select NP_001072.2:n.*267A>T
Search 100 bp 5'
Search 100 bp 3'