Canonical Allele Identifier: CA5424392

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16984264C>T , CM000672.2:g.16984264C>T	GRCh38
NC_000010.10:g.17026263C>T , CM000672.1:g.17026263C>T	GRCh37
NC_000010.9:g.17066269C>T	NCBI36
NG_008967.1:g.150554G>A , LRG_540:g.150554G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4366G>A MANE Select	NP_001072.2:p.Asp1456Asn
ENST00000377833.10:c.4366G>A MANE Select	ENSP00000367064.4:p.Asp1456Asn
NM_001081.3:c.4366G>A , LRG_540t1:c.4366G>A	NP_001072.2:p.Asp1456Asn
ENST00000377833.8:c.4366G>A	ENSP00000367064.4:p.Asp1456Asn
XM_011519708.1:c.4366G>A	XP_011518010.1:p.Asp1456Asn
XM_011519708.2:c.4366G>A	XP_011518010.1:p.Asp1456Asn
XM_011519709.1:c.352G>A	XP_011518011.1:p.Asp118Asn
XM_011519709.2:c.352G>A	XP_011518011.1:p.Asp118Asn
XM_011519710.1:c.328G>A	XP_011518012.1:p.Asp110Asn
XM_011519710.2:c.328G>A	XP_011518012.1:p.Asp110Asn
XM_011519711.1:c.208G>A	XP_011518013.1:p.Asp70Asn
XM_011519711.3:c.208G>A	XP_011518013.1:p.Asp70Asn