Canonical Allele Identifier: CA1893309963

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825001C= , CM000672.2:g.16825001C=	GRCh38
NC_000010.10:g.16867000C= , CM000672.1:g.16867000C=	GRCh37
NC_000010.9:g.16907006C=	NCBI36
NG_008967.1:g.309817G= , LRG_540:g.309817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10846G= MANE Select	ENSP00000367064.4:p.Ala3616=
ENST00000377833.8:c.10846G=	ENSP00000367064.4:p.Ala3616=
NM_001081.3:c.10846G= , LRG_540t1:c.10846G=	NP_001072.2:p.Ala3616=
XM_011519709.1:c.6832G=	XP_011518011.1:p.Ala2278=
XM_011519710.1:c.6808G=	XP_011518012.1:p.Ala2270=
XM_011519711.1:c.6688G=	XP_011518013.1:p.Ala2230=
XM_011519709.2:c.6832G=	XP_011518011.1:p.Ala2278=
XM_011519710.2:c.6808G=	XP_011518012.1:p.Ala2270=
XM_011519711.3:c.6688G=	XP_011518013.1:p.Ala2230=
NM_001081.4:c.10846G= MANE Select	NP_001072.2:p.Ala3616=