Canonical Allele Identifier: CA1893472746

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129744A= , CM000672.2:g.17129744A=	GRCh38
NC_000010.10:g.17171743A= , CM000672.1:g.17171743A=	GRCh37
NC_000010.9:g.17211749A=	NCBI36
NG_008967.1:g.5074T= , LRG_540:g.5074T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.22T= MANE Select	ENSP00000367064.4:p.Phe8=
ENST00000377823.1:c.22T=	ENSP00000367054.1:p.Phe8=
ENST00000377833.8:c.22T=	ENSP00000367064.4:p.Phe8=
NM_001081.3:c.22T= , LRG_540t1:c.22T=	NP_001072.2:p.Phe8=
XM_011519708.1:c.22T=	XP_011518010.1:p.Phe8=
XM_011519708.2:c.22T=	XP_011518010.1:p.Phe8=
NM_001081.4:c.22T= MANE Select	NP_001072.2:p.Phe8=