Canonical Allele Identifier: CA1893309535

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824656A= , CM000672.2:g.16824656A=	GRCh38
NC_000010.10:g.16866655A= , CM000672.1:g.16866655A=	GRCh37
NC_000010.9:g.16906661A=	NCBI36
NG_008967.1:g.310162T= , LRG_540:g.310162T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*319T= MANE Select	ENSP00000367064.4:n.*319T=
ENST00000377833.8:c.*319T=	ENSP00000367064.4:n.*319T=
NM_001081.3:c.*319T= , LRG_540t1:c.*319T=	NP_001072.2:n.*319T=
XM_011519709.1:c.*319T=	XP_011518011.1:n.*319T=
XM_011519710.1:c.*319T=	XP_011518012.1:n.*319T=
XM_011519711.1:c.*319T=	XP_011518013.1:n.*319T=
XM_011519709.2:c.*319T=	XP_011518011.1:n.*319T=
XM_011519710.2:c.*319T=	XP_011518012.1:n.*319T=
XM_011519711.3:c.*319T=	XP_011518013.1:n.*319T=
NM_001081.4:c.*319T= MANE Select	NP_001072.2:n.*319T=