Canonical Allele Identifier: CA1893383850

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16955730C= , CM000672.2:g.16955730C=	GRCh38
NC_000010.10:g.16997729C= , CM000672.1:g.16997729C=	GRCh37
NC_000010.9:g.17037735C=	NCBI36
NG_008967.1:g.179088G= , LRG_540:g.179088G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.4696-1182G= MANE Select	ENSP00000367064.4:n.4696-1182G=
ENST00000377833.8:c.4696-1182G=	ENSP00000367064.4:n.4696-1182G=
NM_001081.3:c.4696-1182G= , LRG_540t1:c.4696-1182G=	NP_001072.2:n.4696-1182G=
XM_011519708.1:c.4696-1182G=	XP_011518010.1:n.4696-1182G=
XM_011519709.1:c.682-1182G=	XP_011518011.1:n.682-1182G=
XM_011519710.1:c.658-1182G=	XP_011518012.1:n.658-1182G=
XM_011519711.1:c.538-1182G=	XP_011518013.1:n.538-1182G=
XM_011519708.2:c.4696-1182G=	XP_011518010.1:n.4696-1182G=
XM_011519709.2:c.682-1182G=	XP_011518011.1:n.682-1182G=
XM_011519710.2:c.658-1182G=	XP_011518012.1:n.658-1182G=
XM_011519711.3:c.538-1182G=	XP_011518013.1:n.538-1182G=
NM_001081.4:c.4696-1182G= MANE Select	NP_001072.2:n.4696-1182G=