Canonical Allele Identifier: CA2501008691

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915817_16915818insG , CM000672.2:g.16915817_16915818insG	GRCh38
NC_000010.10:g.16957816_16957817insG , CM000672.1:g.16957816_16957817insG	GRCh37
NC_000010.9:g.16997822_16997823insG	NCBI36
NG_008967.1:g.219000_219001insC , LRG_540:g.219000_219001insC

Transcript Alleles

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