Canonical Allele Identifier: CA1893371525

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915959T= , CM000672.2:g.16915959T=	GRCh38
NC_000010.10:g.16957958T= , CM000672.1:g.16957958T=	GRCh37
NC_000010.9:g.16997964T=	NCBI36
NG_008967.1:g.218859A= , LRG_540:g.218859A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7072A= MANE Select	ENSP00000367064.4:p.Arg2358=
ENST00000377833.8:c.7072A=	ENSP00000367064.4:p.Arg2358=
NM_001081.3:c.7072A= , LRG_540t1:c.7072A=	NP_001072.2:p.Arg2358=
XM_011519708.1:c.7072A=	XP_011518010.1:p.Arg2358=
XM_011519709.1:c.3058A=	XP_011518011.1:p.Arg1020=
XM_011519710.1:c.3034A=	XP_011518012.1:p.Arg1012=
XM_011519711.1:c.2914A=	XP_011518013.1:p.Arg972=
XM_011519708.2:c.7072A=	XP_011518010.1:p.Arg2358=
XM_011519709.2:c.3058A=	XP_011518011.1:p.Arg1020=
XM_011519710.2:c.3034A=	XP_011518012.1:p.Arg1012=
XM_011519711.3:c.2914A=	XP_011518013.1:p.Arg972=
NM_001081.4:c.7072A= MANE Select	NP_001072.2:p.Arg2358=