Canonical Allele Identifier: CA5422275

Gene: CUBN

Linked Data

• dbSNP Id: rs747501234
• ExAC: 10:16867009 G / A
• gnomAD v2: 10-16867009-G-A
• gnomAD v3: 10-16825010-G-A
• gnomAD v4: 10-16825010-G-A
• MyVariant Identifiers: chr10:g.16867009G>A (hg19) ; chr10:g.16825010G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10837C>T MANE Select	ENSP00000367064.4:p.Arg3613Cys
ENST00000377833.8:c.10837C>T	ENSP00000367064.4:p.Arg3613Cys
NM_001081.3:c.10837C>T , LRG_540t1:c.10837C>T	NP_001072.2:p.Arg3613Cys
XM_011519709.1:c.6823C>T	XP_011518011.1:p.Arg2275Cys
XM_011519710.1:c.6799C>T	XP_011518012.1:p.Arg2267Cys
XM_011519711.1:c.6679C>T	XP_011518013.1:p.Arg2227Cys
XM_011519709.2:c.6823C>T	XP_011518011.1:p.Arg2275Cys
XM_011519710.2:c.6799C>T	XP_011518012.1:p.Arg2267Cys
XM_011519711.3:c.6679C>T	XP_011518013.1:p.Arg2227Cys
NM_001081.4:c.10837C>T MANE Select	NP_001072.2:p.Arg3613Cys