Canonical Allele Identifier: CA1893471273

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17126727_17126728delinsGA , CM000672.2:g.17126727_17126728delinsGA	GRCh38
NC_000010.10:g.17168726_17168727delinsGA , CM000672.1:g.17168726_17168727delinsGA	GRCh37
NC_000010.9:g.17208732_17208733delinsGA	NCBI36
NG_008967.1:g.8090_8091delinsTC , LRG_540:g.8090_8091delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.387+33_387+34delinsTC MANE Select	ENSP00000367064.4:n.387+33_387+34delinsTC...
ENST00000377823.1:c.387+33_387+34delinsTC	ENSP00000367054.1:n.387+33_387+34delinsTC...
ENST00000377833.8:c.387+33_387+34delinsTC	ENSP00000367064.4:n.387+33_387+34delinsTC...
ENST00000433666.5:c.48+33_48+34delinsTC	ENSP00000415970.1:n.48+33_48+34delinsTC
NM_001081.3:c.387+33_387+34delinsTC , LRG_540t1:c.387+33_387+34delinsTC	NP_001072.2:n.387+33_387+34delinsTC
XM_011519708.1:c.387+33_387+34delinsTC	XP_011518010.1:n.387+33_387+34delinsTC
XM_011519708.2:c.387+33_387+34delinsTC	XP_011518010.1:n.387+33_387+34delinsTC
NM_001081.4:c.387+33_387+34delinsTC MANE Select	NP_001072.2:n.387+33_387+34delinsTC