Canonical Allele Identifier: CA1893309600

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824709G= , CM000672.2:g.16824709G=	GRCh38
NC_000010.10:g.16866708G= , CM000672.1:g.16866708G=	GRCh37
NC_000010.9:g.16906714G=	NCBI36
NG_008967.1:g.310109C= , LRG_540:g.310109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*266C= MANE Select	ENSP00000367064.4:n.*266C=
ENST00000377833.8:c.*266C=	ENSP00000367064.4:n.*266C=
NM_001081.3:c.*266C= , LRG_540t1:c.*266C=	NP_001072.2:n.*266C=
XM_011519709.1:c.*266C=	XP_011518011.1:n.*266C=
XM_011519710.1:c.*266C=	XP_011518012.1:n.*266C=
XM_011519711.1:c.*266C=	XP_011518013.1:n.*266C=
XM_011519709.2:c.*266C=	XP_011518011.1:n.*266C=
XM_011519710.2:c.*266C=	XP_011518012.1:n.*266C=
XM_011519711.3:c.*266C=	XP_011518013.1:n.*266C=
NM_001081.4:c.*266C= MANE Select	NP_001072.2:n.*266C=