Canonical Allele Identifier: CA2842296302

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824838A>T , CM000672.2:g.16824838A>T	GRCh38
NC_000010.10:g.16866837A>T , CM000672.1:g.16866837A>T	GRCh37
NC_000010.9:g.16906843A>T	NCBI36
NG_008967.1:g.309980T>A , LRG_540:g.309980T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*137T>A MANE Select	ENSP00000367064.4:n.*137T>A
ENST00000377833.8:c.*137T>A	ENSP00000367064.4:n.*137T>A
NM_001081.3:c.*137T>A , LRG_540t1:c.*137T>A	NP_001072.2:n.*137T>A
XM_011519709.1:c.*137T>A	XP_011518011.1:n.*137T>A
XM_011519710.1:c.*137T>A	XP_011518012.1:n.*137T>A
XM_011519711.1:c.*137T>A	XP_011518013.1:n.*137T>A
XM_011519709.2:c.*137T>A	XP_011518011.1:n.*137T>A
XM_011519710.2:c.*137T>A	XP_011518012.1:n.*137T>A
XM_011519711.3:c.*137T>A	XP_011518013.1:n.*137T>A
NM_001081.4:c.*137T>A MANE Select	NP_001072.2:n.*137T>A