Canonical Allele Identifier: CA10631299
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 299353
ClinVar RCV Id: RCV000373673
dbSNP Id: rs886046861

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824894G>T , CM000672.2:g.16824894G>T GRCh38
NC_000010.10:g.16866893G>T , CM000672.1:g.16866893G>T GRCh37
NC_000010.9:g.16906899G>T NCBI36
NG_008967.1:g.309924C>A , LRG_540:g.309924C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*81C>A MANE Select ENSP00000367064.4:n.*81C>A
ENST00000377833.8:c.*81C>A ENSP00000367064.4:n.*81C>A
NM_001081.3:c.*81C>A , LRG_540t1:c.*81C>A NP_001072.2:n.*81C>A
XM_011519709.1:c.*81C>A XP_011518011.1:n.*81C>A
XM_011519710.1:c.*81C>A XP_011518012.1:n.*81C>A
XM_011519711.1:c.*81C>A XP_011518013.1:n.*81C>A
XM_011519709.2:c.*81C>A XP_011518011.1:n.*81C>A
XM_011519710.2:c.*81C>A XP_011518012.1:n.*81C>A
XM_011519711.3:c.*81C>A XP_011518013.1:n.*81C>A
NM_001081.4:c.*81C>A MANE Select NP_001072.2:n.*81C>A