Canonical Allele Identifier: CA5424418

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16990329C>T , CM000672.2:g.16990329C>T	GRCh38
NC_000010.10:g.17032328C>T , CM000672.1:g.17032328C>T	GRCh37
NC_000010.9:g.17072334C>T	NCBI36
NG_008967.1:g.144489G>A , LRG_540:g.144489G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4350+5G>A MANE Select	NP_001072.2:n.4350+5G>A
ENST00000377833.10:c.4350+5G>A MANE Select	ENSP00000367064.4:n.4350+5G>A
NM_001081.3:c.4350+5G>A , LRG_540t1:c.4350+5G>A	NP_001072.2:n.4350+5G>A
ENST00000377833.8:c.4350+5G>A	ENSP00000367064.4:n.4350+5G>A
XM_011519708.1:c.4350+5G>A	XP_011518010.1:n.4350+5G>A
XM_011519708.2:c.4350+5G>A	XP_011518010.1:n.4350+5G>A
XM_011519709.1:c.336+5G>A	XP_011518011.1:n.336+5G>A
XM_011519709.2:c.336+5G>A	XP_011518011.1:n.336+5G>A
XM_011519710.1:c.312+5G>A	XP_011518012.1:n.312+5G>A
XM_011519710.2:c.312+5G>A	XP_011518012.1:n.312+5G>A
XM_011519711.1:c.192+5G>A	XP_011518013.1:n.192+5G>A
XM_011519711.3:c.192+5G>A	XP_011518013.1:n.192+5G>A