Canonical Allele Identifier: CA10635046

Gene: CUBN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16916034C>T , CM000672.2:g.16916034C>T	GRCh38
NC_000010.10:g.16958033C>T , CM000672.1:g.16958033C>T	GRCh37
NC_000010.9:g.16998039C>T	NCBI36
NG_008967.1:g.218784G>A , LRG_540:g.218784G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7001-4G>A MANE Select	ENSP00000367064.4:n.7001-4G>A
ENST00000377833.8:c.7001-4G>A	ENSP00000367064.4:n.7001-4G>A
NM_001081.3:c.7001-4G>A , LRG_540t1:c.7001-4G>A	NP_001072.2:n.7001-4G>A
XM_011519708.1:c.7001-4G>A	XP_011518010.1:n.7001-4G>A
XM_011519709.1:c.2987-4G>A	XP_011518011.1:n.2987-4G>A
XM_011519710.1:c.2963-4G>A	XP_011518012.1:n.2963-4G>A
XM_011519711.1:c.2843-4G>A	XP_011518013.1:n.2843-4G>A
XM_011519708.2:c.7001-4G>A	XP_011518010.1:n.7001-4G>A
XM_011519709.2:c.2987-4G>A	XP_011518011.1:n.2987-4G>A
XM_011519710.2:c.2963-4G>A	XP_011518012.1:n.2963-4G>A
XM_011519711.3:c.2843-4G>A	XP_011518013.1:n.2843-4G>A
NM_001081.4:c.7001-4G>A MANE Select	NP_001072.2:n.7001-4G>A