Canonical Allele Identifier: CA2536968956

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824649_16824650insAGCT , CM000672.2:g.16824649_16824650insAGCT	GRCh38
NC_000010.10:g.16866648_16866649insAGCT , CM000672.1:g.16866648_16866649insAGCT	GRCh37
NC_000010.9:g.16906654_16906655insAGCT	NCBI36
NG_008967.1:g.310169_310170insGCTA , LRG_540:g.310169_310170insGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*326_*327insGCTA MANE Select	ENSP00000367064.4:n.*326_*327insGCTA
ENST00000377833.8:c.*326_*327insGCTA	ENSP00000367064.4:n.*326_*327insGCTA
NM_001081.3:c.*326_*327insGCTA , LRG_540t1:c.*326_*327insGCTA	NP_001072.2:n.*326_*327insGCTA
XM_011519709.1:c.*326_*327insGCTA	XP_011518011.1:n.*326_*327insGCTA
XM_011519710.1:c.*326_*327insGCTA	XP_011518012.1:n.*326_*327insGCTA
XM_011519711.1:c.*326_*327insGCTA	XP_011518013.1:n.*326_*327insGCTA
XM_011519709.2:c.*326_*327insGCTA	XP_011518011.1:n.*326_*327insGCTA
XM_011519710.2:c.*326_*327insGCTA	XP_011518012.1:n.*326_*327insGCTA
XM_011519711.3:c.*326_*327insGCTA	XP_011518013.1:n.*326_*327insGCTA
NM_001081.4:c.*326_*327insGCTA MANE Select	NP_001072.2:n.*326_*327insGCTA