Canonical Allele Identifier: CA2786794129

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915747_16915760del , CM000672.2:g.16915747_16915760del	GRCh38
NC_000010.10:g.16957746_16957759del , CM000672.1:g.16957746_16957759del	GRCh37
NC_000010.9:g.16997752_16997765del	NCBI36
NG_008967.1:g.219060_219073del , LRG_540:g.219060_219073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7210+63_7210+76del MANE Select	ENSP00000367064.4:n.7210+63_7210+76del
ENST00000377833.8:c.7210+63_7210+76del	ENSP00000367064.4:n.7210+63_7210+76del
NM_001081.3:c.7210+63_7210+76del , LRG_540t1:c.7210+63_7210+76del	NP_001072.2:n.7210+63_7210+76del
XM_011519708.1:c.7210+63_7210+76del	XP_011518010.1:n.7210+63_7210+76del
XM_011519709.1:c.3196+63_3196+76del	XP_011518011.1:n.3196+63_3196+76del
XM_011519710.1:c.3172+63_3172+76del	XP_011518012.1:n.3172+63_3172+76del
XM_011519711.1:c.3052+63_3052+76del	XP_011518013.1:n.3052+63_3052+76del
XM_011519708.2:c.7210+63_7210+76del	XP_011518010.1:n.7210+63_7210+76del
XM_011519709.2:c.3196+63_3196+76del	XP_011518011.1:n.3196+63_3196+76del
XM_011519710.2:c.3172+63_3172+76del	XP_011518012.1:n.3172+63_3172+76del
XM_011519711.3:c.3052+63_3052+76del	XP_011518013.1:n.3052+63_3052+76del
NM_001081.4:c.7210+63_7210+76del MANE Select	NP_001072.2:n.7210+63_7210+76del