Canonical Allele Identifier: CA1893472747

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129745A= , CM000672.2:g.17129745A=	GRCh38
NC_000010.10:g.17171744A= , CM000672.1:g.17171744A=	GRCh37
NC_000010.9:g.17211750A=	NCBI36
NG_008967.1:g.5073T= , LRG_540:g.5073T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.21T= MANE Select	ENSP00000367064.4:p.Pro7=
ENST00000377823.1:c.21T=	ENSP00000367054.1:p.Pro7=
ENST00000377833.8:c.21T=	ENSP00000367064.4:p.Pro7=
NM_001081.3:c.21T= , LRG_540t1:c.21T=	NP_001072.2:p.Pro7=
XM_011519708.1:c.21T=	XP_011518010.1:p.Pro7=
XM_011519708.2:c.21T=	XP_011518010.1:p.Pro7=
NM_001081.4:c.21T= MANE Select	NP_001072.2:p.Pro7=