Canonical Allele Identifier: CA1893371477

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915847A= , CM000672.2:g.16915847A=	GRCh38
NC_000010.10:g.16957846A= , CM000672.1:g.16957846A=	GRCh37
NC_000010.9:g.16997852A=	NCBI36
NG_008967.1:g.218971T= , LRG_540:g.218971T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7184T= MANE Select	ENSP00000367064.4:p.Val2395=
ENST00000377833.8:c.7184T=	ENSP00000367064.4:p.Val2395=
NM_001081.3:c.7184T= , LRG_540t1:c.7184T=	NP_001072.2:p.Val2395=
XM_011519708.1:c.7184T=	XP_011518010.1:p.Val2395=
XM_011519709.1:c.3170T=	XP_011518011.1:p.Val1057=
XM_011519710.1:c.3146T=	XP_011518012.1:p.Val1049=
XM_011519711.1:c.3026T=	XP_011518013.1:p.Val1009=
XM_011519708.2:c.7184T=	XP_011518010.1:p.Val2395=
XM_011519709.2:c.3170T=	XP_011518011.1:p.Val1057=
XM_011519710.2:c.3146T=	XP_011518012.1:p.Val1049=
XM_011519711.3:c.3026T=	XP_011518013.1:p.Val1009=
NM_001081.4:c.7184T= MANE Select	NP_001072.2:p.Val2395=