Canonical Allele Identifier: CA1893309700
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1838724098
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824773G>T , CM000672.2:g.16824773G>T GRCh38
NC_000010.10:g.16866772G>T , CM000672.1:g.16866772G>T GRCh37
NC_000010.9:g.16906778G>T NCBI36
NG_008967.1:g.310045C>A , LRG_540:g.310045C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*202C>A MANE Select ENSP00000367064.4:n.*202C>A
ENST00000377833.8:c.*202C>A ENSP00000367064.4:n.*202C>A
NM_001081.3:c.*202C>A , LRG_540t1:c.*202C>A NP_001072.2:n.*202C>A
XM_011519709.1:c.*202C>A XP_011518011.1:n.*202C>A
XM_011519710.1:c.*202C>A XP_011518012.1:n.*202C>A
XM_011519711.1:c.*202C>A XP_011518013.1:n.*202C>A
XM_011519709.2:c.*202C>A XP_011518011.1:n.*202C>A
XM_011519710.2:c.*202C>A XP_011518012.1:n.*202C>A
XM_011519711.3:c.*202C>A XP_011518013.1:n.*202C>A
NM_001081.4:c.*202C>A MANE Select NP_001072.2:n.*202C>A
Search 100 bp 5'
Search 100 bp 3'