Canonical Allele Identifier: CA1893309989

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825013G= , CM000672.2:g.16825013G=	GRCh38
NC_000010.10:g.16867012G= , CM000672.1:g.16867012G=	GRCh37
NC_000010.9:g.16907018G=	NCBI36
NG_008967.1:g.309805C= , LRG_540:g.309805C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10834C= MANE Select	ENSP00000367064.4:p.Arg3612=
ENST00000377833.8:c.10834C=	ENSP00000367064.4:p.Arg3612=
NM_001081.3:c.10834C= , LRG_540t1:c.10834C=	NP_001072.2:p.Arg3612=
XM_011519709.1:c.6820C=	XP_011518011.1:p.Arg2274=
XM_011519710.1:c.6796C=	XP_011518012.1:p.Arg2266=
XM_011519711.1:c.6676C=	XP_011518013.1:p.Arg2226=
XM_011519709.2:c.6820C=	XP_011518011.1:p.Arg2274=
XM_011519710.2:c.6796C=	XP_011518012.1:p.Arg2266=
XM_011519711.3:c.6676C=	XP_011518013.1:p.Arg2226=
NM_001081.4:c.10834C= MANE Select	NP_001072.2:p.Arg3612=