Canonical Allele Identifier: CA376169621

Gene: CUBN

Linked Data

• dbSNP Id: rs1837263630
• gnomAD v4: 10-17129134-T-C
• MyVariant Identifiers: chr10:g.17171133T>C (hg19) ; chr10:g.17129134T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129134T>C , CM000672.2:g.17129134T>C	GRCh38
NC_000010.10:g.17171133T>C , CM000672.1:g.17171133T>C	GRCh37
NC_000010.9:g.17211139T>C	NCBI36
NG_008967.1:g.5684A>G , LRG_540:g.5684A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.239A>G MANE Select	ENSP00000367064.4:p.Glu80Gly
ENST00000377823.1:c.239A>G	ENSP00000367054.1:p.Glu80Gly
ENST00000377833.8:c.239A>G	ENSP00000367064.4:p.Glu80Gly
NM_001081.3:c.239A>G , LRG_540t1:c.239A>G	NP_001072.2:p.Glu80Gly
XM_011519708.1:c.239A>G	XP_011518010.1:p.Glu80Gly
XM_011519708.2:c.239A>G	XP_011518010.1:p.Glu80Gly
NM_001081.4:c.239A>G MANE Select	NP_001072.2:p.Glu80Gly