Canonical Allele Identifier: CA1893431258

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17019886G= , CM000672.2:g.17019886G=	GRCh38
NC_000010.10:g.17061885G= , CM000672.1:g.17061885G=	GRCh37
NC_000010.9:g.17101891G=	NCBI36
NG_008967.1:g.114932C= , LRG_540:g.114932C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4115C= MANE Select	NP_001072.2:p.Thr1372=
ENST00000377833.10:c.4115C= MANE Select	ENSP00000367064.4:p.Thr1372=
NM_001081.3:c.4115C= , LRG_540t1:c.4115C=	NP_001072.2:p.Thr1372=
ENST00000377833.8:c.4115C=	ENSP00000367064.4:p.Thr1372=
XM_011519708.1:c.4115C=	XP_011518010.1:p.Thr1372=
XM_011519708.2:c.4115C=	XP_011518010.1:p.Thr1372=
XM_011519709.1:c.101C=	XP_011518011.1:p.Thr34=
XM_011519709.2:c.101C=	XP_011518011.1:p.Thr34=
XM_011519710.1:c.77C=	XP_011518012.1:p.Thr26=
XM_011519710.2:c.77C=	XP_011518012.1:p.Thr26=