Canonical Allele Identifier: CA10635021
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 299343
ClinVar RCV Id: RCV000315242
dbSNP Id: rs886046857

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824678G>A , CM000672.2:g.16824678G>A GRCh38
NC_000010.10:g.16866677G>A , CM000672.1:g.16866677G>A GRCh37
NC_000010.9:g.16906683G>A NCBI36
NG_008967.1:g.310140C>T , LRG_540:g.310140C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*297C>T MANE Select ENSP00000367064.4:n.*297C>T
ENST00000377833.8:c.*297C>T ENSP00000367064.4:n.*297C>T
NM_001081.3:c.*297C>T , LRG_540t1:c.*297C>T NP_001072.2:n.*297C>T
XM_011519709.1:c.*297C>T XP_011518011.1:n.*297C>T
XM_011519710.1:c.*297C>T XP_011518012.1:n.*297C>T
XM_011519711.1:c.*297C>T XP_011518013.1:n.*297C>T
XM_011519709.2:c.*297C>T XP_011518011.1:n.*297C>T
XM_011519710.2:c.*297C>T XP_011518012.1:n.*297C>T
XM_011519711.3:c.*297C>T XP_011518013.1:n.*297C>T
NM_001081.4:c.*297C>T MANE Select NP_001072.2:n.*297C>T