Canonical Allele Identifier: CA662288896

Gene: CUBN

Linked Data

• dbSNP Id: rs1339873281
• gnomAD v3: 10-16824863-C-T
• gnomAD v4: 10-16824863-C-T
• MyVariant Identifiers: chr10:g.16866862C>T (hg19) ; chr10:g.16824863C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824863C>T , CM000672.2:g.16824863C>T	GRCh38
NC_000010.10:g.16866862C>T , CM000672.1:g.16866862C>T	GRCh37
NC_000010.9:g.16906868C>T	NCBI36
NG_008967.1:g.309955G>A , LRG_540:g.309955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*112G>A MANE Select	ENSP00000367064.4:n.*112G>A
ENST00000377833.8:c.*112G>A	ENSP00000367064.4:n.*112G>A
NM_001081.3:c.*112G>A , LRG_540t1:c.*112G>A	NP_001072.2:n.*112G>A
XM_011519709.1:c.*112G>A	XP_011518011.1:n.*112G>A
XM_011519710.1:c.*112G>A	XP_011518012.1:n.*112G>A
XM_011519711.1:c.*112G>A	XP_011518013.1:n.*112G>A
XM_011519709.2:c.*112G>A	XP_011518011.1:n.*112G>A
XM_011519710.2:c.*112G>A	XP_011518012.1:n.*112G>A
XM_011519711.3:c.*112G>A	XP_011518013.1:n.*112G>A
NM_001081.4:c.*112G>A MANE Select	NP_001072.2:n.*112G>A