Canonical Allele Identifier: CA2574500104
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs2131293055

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824920G>C , CM000672.2:g.16824920G>C GRCh38
NC_000010.10:g.16866919G>C , CM000672.1:g.16866919G>C GRCh37
NC_000010.9:g.16906925G>C NCBI36
NG_008967.1:g.309898C>G , LRG_540:g.309898C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*55C>G MANE Select ENSP00000367064.4:n.*55C>G
ENST00000377833.8:c.*55C>G ENSP00000367064.4:n.*55C>G
NM_001081.3:c.*55C>G , LRG_540t1:c.*55C>G NP_001072.2:n.*55C>G
XM_011519709.1:c.*55C>G XP_011518011.1:n.*55C>G
XM_011519710.1:c.*55C>G XP_011518012.1:n.*55C>G
XM_011519711.1:c.*55C>G XP_011518013.1:n.*55C>G
XM_011519709.2:c.*55C>G XP_011518011.1:n.*55C>G
XM_011519710.2:c.*55C>G XP_011518012.1:n.*55C>G
XM_011519711.3:c.*55C>G XP_011518013.1:n.*55C>G
NM_001081.4:c.*55C>G MANE Select NP_001072.2:n.*55C>G