Canonical Allele Identifier: CA2721031495

Gene: CUBN

Linked Data

• dbSNP Id: rs2131842090

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17065415G>C , CM000672.2:g.17065415G>C	GRCh38
NC_000010.10:g.17107414G>C , CM000672.1:g.17107414G>C	GRCh37
NC_000010.9:g.17147420G>C	NCBI36
NG_008967.1:g.69403C>G , LRG_540:g.69403C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.3139+93C>G MANE Select	ENSP00000367064.4:n.3139+93C>G
ENST00000377833.8:c.3139+93C>G	ENSP00000367064.4:n.3139+93C>G
NM_001081.3:c.3139+93C>G , LRG_540t1:c.3139+93C>G	NP_001072.2:n.3139+93C>G
XM_011519708.1:c.3139+93C>G	XP_011518010.1:n.3139+93C>G
XM_011519708.2:c.3139+93C>G	XP_011518010.1:n.3139+93C>G
NM_001081.4:c.3139+93C>G MANE Select	NP_001072.2:n.3139+93C>G