Canonical Allele Identifier: CA925385061

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915818_16915819insCGGCG , CM000672.2:g.16915818_16915819insCGGCG	GRCh38
NC_000010.10:g.16957817_16957818insCGGCG , CM000672.1:g.16957817_16957818insCGGCG	GRCh37
NC_000010.9:g.16997823_16997824insCGGCG	NCBI36
NG_008967.1:g.218999_219000insCGCCG , LRG_540:g.218999_219000insCGCCG

Transcript Alleles

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