Canonical Allele Identifier: CA1893371388

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915614G= , CM000672.2:g.16915614G=	GRCh38
NC_000010.10:g.16957613G= , CM000672.1:g.16957613G=	GRCh37
NC_000010.9:g.16997619G=	NCBI36
NG_008967.1:g.219204C= , LRG_540:g.219204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7210+207C= MANE Select	ENSP00000367064.4:n.7210+207C=
ENST00000377833.8:c.7210+207C=	ENSP00000367064.4:n.7210+207C=
NM_001081.3:c.7210+207C= , LRG_540t1:c.7210+207C=	NP_001072.2:n.7210+207C=
XM_011519708.1:c.7210+207C=	XP_011518010.1:n.7210+207C=
XM_011519709.1:c.3196+207C=	XP_011518011.1:n.3196+207C=
XM_011519710.1:c.3172+207C=	XP_011518012.1:n.3172+207C=
XM_011519711.1:c.3052+207C=	XP_011518013.1:n.3052+207C=
XM_011519708.2:c.7210+207C=	XP_011518010.1:n.7210+207C=
XM_011519709.2:c.3196+207C=	XP_011518011.1:n.3196+207C=
XM_011519710.2:c.3172+207C=	XP_011518012.1:n.3172+207C=
XM_011519711.3:c.3052+207C=	XP_011518013.1:n.3052+207C=
NM_001081.4:c.7210+207C= MANE Select	NP_001072.2:n.7210+207C=