Canonical Allele Identifier: CA925380303
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1486449340
gnomAD v3: 10-16824836-C-G
gnomAD v4: 10-16824836-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824836C>G , CM000672.2:g.16824836C>G GRCh38
NC_000010.10:g.16866835C>G , CM000672.1:g.16866835C>G GRCh37
NC_000010.9:g.16906841C>G NCBI36
NG_008967.1:g.309982G>C , LRG_540:g.309982G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*139G>C MANE Select ENSP00000367064.4:n.*139G>C
ENST00000377833.8:c.*139G>C ENSP00000367064.4:n.*139G>C
NM_001081.3:c.*139G>C , LRG_540t1:c.*139G>C NP_001072.2:n.*139G>C
XM_011519709.1:c.*139G>C XP_011518011.1:n.*139G>C
XM_011519710.1:c.*139G>C XP_011518012.1:n.*139G>C
XM_011519711.1:c.*139G>C XP_011518013.1:n.*139G>C
XM_011519709.2:c.*139G>C XP_011518011.1:n.*139G>C
XM_011519710.2:c.*139G>C XP_011518012.1:n.*139G>C
XM_011519711.3:c.*139G>C XP_011518013.1:n.*139G>C
NM_001081.4:c.*139G>C MANE Select NP_001072.2:n.*139G>C
Search 100 bp 5'
Search 100 bp 3'