Canonical Allele Identifier: CA1893361695

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16877053T= , CM000672.2:g.16877053T=	GRCh38
NC_000010.10:g.16919052T= , CM000672.1:g.16919052T=	GRCh37
NC_000010.9:g.16959058T=	NCBI36
NG_008967.1:g.257765A= , LRG_540:g.257765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.8950A= MANE Select	ENSP00000367064.4:p.Ile2984=
ENST00000377833.8:c.8950A=	ENSP00000367064.4:p.Ile2984=
NM_001081.3:c.8950A= , LRG_540t1:c.8950A=	NP_001072.2:p.Ile2984=
XM_011519709.1:c.4936A=	XP_011518011.1:p.Ile1646=
XM_011519710.1:c.4912A=	XP_011518012.1:p.Ile1638=
XM_011519711.1:c.4792A=	XP_011518013.1:p.Ile1598=
XM_011519709.2:c.4936A=	XP_011518011.1:p.Ile1646=
XM_011519710.2:c.4912A=	XP_011518012.1:p.Ile1638=
XM_011519711.3:c.4792A=	XP_011518013.1:p.Ile1598=
NM_001081.4:c.8950A= MANE Select	NP_001072.2:p.Ile2984=