Canonical Allele Identifier: CA10628276

Gene: CUBN

Linked Data

• ClinVar Variation Id: 299349
• ClinVar RCV Id: RCV000322119
• dbSNP Id: rs558891678
• gnomAD v3: 10-16824813-C-T
• gnomAD v4: 10-16824813-C-T
• MyVariant Identifiers: chr10:g.16866812C>T (hg19) ; chr10:g.16824813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824813C>T , CM000672.2:g.16824813C>T	GRCh38
NC_000010.10:g.16866812C>T , CM000672.1:g.16866812C>T	GRCh37
NC_000010.9:g.16906818C>T	NCBI36
NG_008967.1:g.310005G>A , LRG_540:g.310005G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.*162G>A MANE Select	ENSP00000367064.4:n.*162G>A
ENST00000377833.8:c.*162G>A	ENSP00000367064.4:n.*162G>A
NM_001081.3:c.*162G>A , LRG_540t1:c.*162G>A	NP_001072.2:n.*162G>A
XM_011519709.1:c.*162G>A	XP_011518011.1:n.*162G>A
XM_011519710.1:c.*162G>A	XP_011518012.1:n.*162G>A
XM_011519711.1:c.*162G>A	XP_011518013.1:n.*162G>A
XM_011519709.2:c.*162G>A	XP_011518011.1:n.*162G>A
XM_011519710.2:c.*162G>A	XP_011518012.1:n.*162G>A
XM_011519711.3:c.*162G>A	XP_011518013.1:n.*162G>A
NM_001081.4:c.*162G>A MANE Select	NP_001072.2:n.*162G>A