Canonical Allele Identifier: CA2608400553

Gene: CUBN

Linked Data

• gnomAD v4: 10-17065372-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17065372C>A , CM000672.2:g.17065372C>A	GRCh38
NC_000010.10:g.17107371C>A , CM000672.1:g.17107371C>A	GRCh37
NC_000010.9:g.17147377C>A	NCBI36
NG_008967.1:g.69446G>T , LRG_540:g.69446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.3139+136G>T MANE Select	ENSP00000367064.4:n.3139+136G>T
ENST00000377833.8:c.3139+136G>T	ENSP00000367064.4:n.3139+136G>T
NM_001081.3:c.3139+136G>T , LRG_540t1:c.3139+136G>T	NP_001072.2:n.3139+136G>T
XM_011519708.1:c.3139+136G>T	XP_011518010.1:n.3139+136G>T
XM_011519708.2:c.3139+136G>T	XP_011518010.1:n.3139+136G>T
NM_001081.4:c.3139+136G>T MANE Select	NP_001072.2:n.3139+136G>T