Canonical Allele Identifier: CA5423570

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16919960T>C , CM000672.2:g.16919960T>C	GRCh38
NC_000010.10:g.16961959T>C , CM000672.1:g.16961959T>C	GRCh37
NC_000010.9:g.17001965T>C	NCBI36
NG_008967.1:g.214858A>G , LRG_540:g.214858A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.6821+3A>G MANE Select	NP_001072.2:n.6821+3A>G
ENST00000377833.10:c.6821+3A>G MANE Select	ENSP00000367064.4:n.6821+3A>G
NM_001081.3:c.6821+3A>G , LRG_540t1:c.6821+3A>G	NP_001072.2:n.6821+3A>G
ENST00000377833.8:c.6821+3A>G	ENSP00000367064.4:n.6821+3A>G
XM_011519708.1:c.6821+3A>G	XP_011518010.1:n.6821+3A>G
XM_011519708.2:c.6821+3A>G	XP_011518010.1:n.6821+3A>G
XM_011519709.1:c.2807+3A>G	XP_011518011.1:n.2807+3A>G
XM_011519709.2:c.2807+3A>G	XP_011518011.1:n.2807+3A>G
XM_011519710.1:c.2783+3A>G	XP_011518012.1:n.2783+3A>G
XM_011519710.2:c.2783+3A>G	XP_011518012.1:n.2783+3A>G
XM_011519711.1:c.2663+3A>G	XP_011518013.1:n.2663+3A>G
XM_011519711.3:c.2663+3A>G	XP_011518013.1:n.2663+3A>G