Canonical Allele Identifier: CA376118638

Gene: CUBN

Linked Data

• COSMIC: COSM6065635
• MyVariant Identifiers: chr10:g.16867009G>T (hg19) ; chr10:g.16825010G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825010G>T , CM000672.2:g.16825010G>T	GRCh38
NC_000010.10:g.16867009G>T , CM000672.1:g.16867009G>T	GRCh37
NC_000010.9:g.16907015G>T	NCBI36
NG_008967.1:g.309808C>A , LRG_540:g.309808C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10837C>A MANE Select	ENSP00000367064.4:p.Arg3613Ser
ENST00000377833.8:c.10837C>A	ENSP00000367064.4:p.Arg3613Ser
NM_001081.3:c.10837C>A , LRG_540t1:c.10837C>A	NP_001072.2:p.Arg3613Ser
XM_011519709.1:c.6823C>A	XP_011518011.1:p.Arg2275Ser
XM_011519710.1:c.6799C>A	XP_011518012.1:p.Arg2267Ser
XM_011519711.1:c.6679C>A	XP_011518013.1:p.Arg2227Ser
XM_011519709.2:c.6823C>A	XP_011518011.1:p.Arg2275Ser
XM_011519710.2:c.6799C>A	XP_011518012.1:p.Arg2267Ser
XM_011519711.3:c.6679C>A	XP_011518013.1:p.Arg2227Ser
NM_001081.4:c.10837C>A MANE Select	NP_001072.2:p.Arg3613Ser