Canonical Allele Identifier: CA1893309673

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824768C= , CM000672.2:g.16824768C=	GRCh38
NC_000010.10:g.16866767C= , CM000672.1:g.16866767C=	GRCh37
NC_000010.9:g.16906773C=	NCBI36
NG_008967.1:g.310050G= , LRG_540:g.310050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*207G= MANE Select	ENSP00000367064.4:n.*207G=
ENST00000377833.8:c.*207G=	ENSP00000367064.4:n.*207G=
NM_001081.3:c.*207G= , LRG_540t1:c.*207G=	NP_001072.2:n.*207G=
XM_011519709.1:c.*207G=	XP_011518011.1:n.*207G=
XM_011519710.1:c.*207G=	XP_011518012.1:n.*207G=
XM_011519711.1:c.*207G=	XP_011518013.1:n.*207G=
XM_011519709.2:c.*207G=	XP_011518011.1:n.*207G=
XM_011519710.2:c.*207G=	XP_011518012.1:n.*207G=
XM_011519711.3:c.*207G=	XP_011518013.1:n.*207G=
NM_001081.4:c.*207G= MANE Select	NP_001072.2:n.*207G=