Canonical Allele Identifier: CA925375088

Gene: CUBN

Linked Data

• dbSNP Id: rs1843045416
• gnomAD v3: 10-16955750-TA-T
• gnomAD v4: 10-16955750-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16955752del , CM000672.2:g.16955752del	GRCh38
NC_000010.10:g.16997751del , CM000672.1:g.16997751del	GRCh37
NC_000010.9:g.17037757del	NCBI36
NG_008967.1:g.179067del , LRG_540:g.179067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.4696-1203del MANE Select	ENSP00000367064.4:n.4696-1203del
ENST00000377833.8:c.4696-1203del	ENSP00000367064.4:n.4696-1203del
NM_001081.3:c.4696-1203del , LRG_540t1:c.4696-1203del	NP_001072.2:n.4696-1203del
XM_011519708.1:c.4696-1203del	XP_011518010.1:n.4696-1203del
XM_011519709.1:c.682-1203del	XP_011518011.1:n.682-1203del
XM_011519710.1:c.658-1203del	XP_011518012.1:n.658-1203del
XM_011519711.1:c.538-1203del	XP_011518013.1:n.538-1203del
XM_011519708.2:c.4696-1203del	XP_011518010.1:n.4696-1203del
XM_011519709.2:c.682-1203del	XP_011518011.1:n.682-1203del
XM_011519710.2:c.658-1203del	XP_011518012.1:n.658-1203del
XM_011519711.3:c.538-1203del	XP_011518013.1:n.538-1203del
NM_001081.4:c.4696-1203del MANE Select	NP_001072.2:n.4696-1203del