Canonical Allele Identifier: CA2608404917

Gene: CUBN

Linked Data

• gnomAD v4: 10-17126641-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17126646del , CM000672.2:g.17126646del	GRCh38
NC_000010.10:g.17168645del , CM000672.1:g.17168645del	GRCh37
NC_000010.9:g.17208651del	NCBI36
NG_008967.1:g.8176del , LRG_540:g.8176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.387+119del MANE Select	ENSP00000367064.4:n.387+119del
ENST00000377823.1:c.387+119del	ENSP00000367054.1:n.387+119del
ENST00000377833.8:c.387+119del	ENSP00000367064.4:n.387+119del
ENST00000433666.5:c.48+119del	ENSP00000415970.1:n.48+119del
NM_001081.3:c.387+119del , LRG_540t1:c.387+119del	NP_001072.2:n.387+119del
XM_011519708.1:c.387+119del	XP_011518010.1:n.387+119del
XM_011519708.2:c.387+119del	XP_011518010.1:n.387+119del
NM_001081.4:c.387+119del MANE Select	NP_001072.2:n.387+119del