Canonical Allele Identifier: CA1893371478

Gene: CUBN

Linked Data

• dbSNP Id: rs1729864646

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915848del , CM000672.2:g.16915848del	GRCh38
NC_000010.10:g.16957847del , CM000672.1:g.16957847del	GRCh37
NC_000010.9:g.16997853del	NCBI36
NG_008967.1:g.218970del , LRG_540:g.218970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7183del MANE Select	ENSP00000367064.4:p.Val2395TrpfsTer25
ENST00000377833.8:c.7183del	ENSP00000367064.4:p.Val2395TrpfsTer25
NM_001081.3:c.7183del , LRG_540t1:c.7183del	NP_001072.2:p.Val2395TrpfsTer25
XM_011519708.1:c.7183del	XP_011518010.1:p.Val2395TrpfsTer25
XM_011519709.1:c.3169del	XP_011518011.1:p.Val1057TrpfsTer25
XM_011519710.1:c.3145del	XP_011518012.1:p.Val1049TrpfsTer25
XM_011519711.1:c.3025del	XP_011518013.1:p.Val1009TrpfsTer25
XM_011519708.2:c.7183del	XP_011518010.1:p.Val2395TrpfsTer25
XM_011519709.2:c.3169del	XP_011518011.1:p.Val1057TrpfsTer25
XM_011519710.2:c.3145del	XP_011518012.1:p.Val1049TrpfsTer25
XM_011519711.3:c.3025del	XP_011518013.1:p.Val1009TrpfsTer25
NM_001081.4:c.7183del MANE Select	NP_001072.2:p.Val2395TrpfsTer25