Canonical Allele Identifier: CA5422824

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16876925G>A , CM000672.2:g.16876925G>A	GRCh38
NC_000010.10:g.16918924G>A , CM000672.1:g.16918924G>A	GRCh37
NC_000010.9:g.16958930G>A	NCBI36
NG_008967.1:g.257893C>T , LRG_540:g.257893C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9078C>T MANE Select	NP_001072.2:p.Phe3026=
ENST00000377833.10:c.9078C>T MANE Select	ENSP00000367064.4:p.Phe3026=
NM_001081.3:c.9078C>T , LRG_540t1:c.9078C>T	NP_001072.2:p.Phe3026=
ENST00000377833.8:c.9078C>T	ENSP00000367064.4:p.Phe3026=
XM_011519709.1:c.5064C>T	XP_011518011.1:p.Phe1688=
XM_011519709.2:c.5064C>T	XP_011518011.1:p.Phe1688=
XM_011519710.1:c.5040C>T	XP_011518012.1:p.Phe1680=
XM_011519710.2:c.5040C>T	XP_011518012.1:p.Phe1680=
XM_011519711.1:c.4920C>T	XP_011518013.1:p.Phe1640=
XM_011519711.3:c.4920C>T	XP_011518013.1:p.Phe1640=