Canonical Allele Identifier: CA1893313302

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828293T= , CM000672.2:g.16828293T=	GRCh38
NC_000010.10:g.16870292T= , CM000672.1:g.16870292T=	GRCh37
NC_000010.9:g.16910298T=	NCBI36
NG_008967.1:g.306525A= , LRG_540:g.306525A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10764+512A= MANE Select	NP_001072.2:n.10764+512A=
ENST00000377833.10:c.10764+512A= MANE Select	ENSP00000367064.4:n.10764+512A=
NM_001081.3:c.10764+512A= , LRG_540t1:c.10764+512A=	NP_001072.2:n.10764+512A=
ENST00000377833.8:c.10764+512A=	ENSP00000367064.4:n.10764+512A=
XM_011519709.1:c.6750+512A=	XP_011518011.1:n.6750+512A=
XM_011519709.2:c.6750+512A=	XP_011518011.1:n.6750+512A=
XM_011519710.1:c.6726+512A=	XP_011518012.1:n.6726+512A=
XM_011519710.2:c.6726+512A=	XP_011518012.1:n.6726+512A=
XM_011519711.1:c.6606+512A=	XP_011518013.1:n.6606+512A=
XM_011519711.3:c.6606+512A=	XP_011518013.1:n.6606+512A=