Canonical Allele Identifier: CA10635349
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 299357
ClinVar RCV Id: RCV000294343
dbSNP Id: rs886046862

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828817T>A , CM000672.2:g.16828817T>A GRCh38
NC_000010.10:g.16870816T>A , CM000672.1:g.16870816T>A GRCh37
NC_000010.9:g.16910822T>A NCBI36
NG_008967.1:g.306001A>T , LRG_540:g.306001A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10752A>T MANE Select ENSP00000367064.4:p.Pro3584=
ENST00000377833.8:c.10752A>T ENSP00000367064.4:p.Pro3584=
NM_001081.3:c.10752A>T , LRG_540t1:c.10752A>T NP_001072.2:p.Pro3584=
XM_011519709.1:c.6738A>T XP_011518011.1:p.Pro2246=
XM_011519710.1:c.6714A>T XP_011518012.1:p.Pro2238=
XM_011519711.1:c.6594A>T XP_011518013.1:p.Pro2198=
XM_011519709.2:c.6738A>T XP_011518011.1:p.Pro2246=
XM_011519710.2:c.6714A>T XP_011518012.1:p.Pro2238=
XM_011519711.3:c.6594A>T XP_011518013.1:p.Pro2198=
NM_001081.4:c.10752A>T MANE Select NP_001072.2:p.Pro3584=