Canonical Allele Identifier: CA1893431238

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17019833C= , CM000672.2:g.17019833C=	GRCh38
NC_000010.10:g.17061832C= , CM000672.1:g.17061832C=	GRCh37
NC_000010.9:g.17101838C=	NCBI36
NG_008967.1:g.114985G= , LRG_540:g.114985G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4168G= MANE Select	NP_001072.2:p.Gly1390=
ENST00000377833.10:c.4168G= MANE Select	ENSP00000367064.4:p.Gly1390=
NM_001081.3:c.4168G= , LRG_540t1:c.4168G=	NP_001072.2:p.Gly1390=
ENST00000377833.8:c.4168G=	ENSP00000367064.4:p.Gly1390=
XM_011519708.1:c.4168G=	XP_011518010.1:p.Gly1390=
XM_011519708.2:c.4168G=	XP_011518010.1:p.Gly1390=
XM_011519709.1:c.154G=	XP_011518011.1:p.Gly52=
XM_011519709.2:c.154G=	XP_011518011.1:p.Gly52=
XM_011519710.1:c.130G=	XP_011518012.1:p.Gly44=
XM_011519710.2:c.130G=	XP_011518012.1:p.Gly44=