Canonical Allele Identifier: CA376145888

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957818A>T (hg19) ; chr10:g.16915819A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915819A>T , CM000672.2:g.16915819A>T	GRCh38
NC_000010.10:g.16957818A>T , CM000672.1:g.16957818A>T	GRCh37
NC_000010.9:g.16997824A>T	NCBI36
NG_008967.1:g.218999T>A , LRG_540:g.218999T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7210+2T>A MANE Select	ENSP00000367064.4:n.7210+2T>A
ENST00000377833.8:c.7210+2T>A	ENSP00000367064.4:n.7210+2T>A
NM_001081.3:c.7210+2T>A , LRG_540t1:c.7210+2T>A	NP_001072.2:n.7210+2T>A
XM_011519708.1:c.7210+2T>A	XP_011518010.1:n.7210+2T>A
XM_011519709.1:c.3196+2T>A	XP_011518011.1:n.3196+2T>A
XM_011519710.1:c.3172+2T>A	XP_011518012.1:n.3172+2T>A
XM_011519711.1:c.3052+2T>A	XP_011518013.1:n.3052+2T>A
XM_011519708.2:c.7210+2T>A	XP_011518010.1:n.7210+2T>A
XM_011519709.2:c.3196+2T>A	XP_011518011.1:n.3196+2T>A
XM_011519710.2:c.3172+2T>A	XP_011518012.1:n.3172+2T>A
XM_011519711.3:c.3052+2T>A	XP_011518013.1:n.3052+2T>A
NM_001081.4:c.7210+2T>A MANE Select	NP_001072.2:n.7210+2T>A