Canonical Allele Identifier: CA2608396046

Gene: CUBN

Linked Data

• gnomAD v4: 10-16824653-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824653T>A , CM000672.2:g.16824653T>A	GRCh38
NC_000010.10:g.16866652T>A , CM000672.1:g.16866652T>A	GRCh37
NC_000010.9:g.16906658T>A	NCBI36
NG_008967.1:g.310165A>T , LRG_540:g.310165A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*322A>T MANE Select	ENSP00000367064.4:n.*322A>T
ENST00000377833.8:c.*322A>T	ENSP00000367064.4:n.*322A>T
NM_001081.3:c.*322A>T , LRG_540t1:c.*322A>T	NP_001072.2:n.*322A>T
XM_011519709.1:c.*322A>T	XP_011518011.1:n.*322A>T
XM_011519710.1:c.*322A>T	XP_011518012.1:n.*322A>T
XM_011519711.1:c.*322A>T	XP_011518013.1:n.*322A>T
XM_011519709.2:c.*322A>T	XP_011518011.1:n.*322A>T
XM_011519710.2:c.*322A>T	XP_011518012.1:n.*322A>T
XM_011519711.3:c.*322A>T	XP_011518013.1:n.*322A>T
NM_001081.4:c.*322A>T MANE Select	NP_001072.2:n.*322A>T