Canonical Allele Identifier: CA1893371492

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915876C= , CM000672.2:g.16915876C=	GRCh38
NC_000010.10:g.16957875C= , CM000672.1:g.16957875C=	GRCh37
NC_000010.9:g.16997881C=	NCBI36
NG_008967.1:g.218942G= , LRG_540:g.218942G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.7155G= MANE Select	ENSP00000367064.4:p.Gln2385=
ENST00000377833.8:c.7155G=	ENSP00000367064.4:p.Gln2385=
NM_001081.3:c.7155G= , LRG_540t1:c.7155G=	NP_001072.2:p.Gln2385=
XM_011519708.1:c.7155G=	XP_011518010.1:p.Gln2385=
XM_011519709.1:c.3141G=	XP_011518011.1:p.Gln1047=
XM_011519710.1:c.3117G=	XP_011518012.1:p.Gln1039=
XM_011519711.1:c.2997G=	XP_011518013.1:p.Gln999=
XM_011519708.2:c.7155G=	XP_011518010.1:p.Gln2385=
XM_011519709.2:c.3141G=	XP_011518011.1:p.Gln1047=
XM_011519710.2:c.3117G=	XP_011518012.1:p.Gln1039=
XM_011519711.3:c.2997G=	XP_011518013.1:p.Gln999=
NM_001081.4:c.7155G= MANE Select	NP_001072.2:p.Gln2385=