Canonical Allele Identifier: CA1893309725
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1838724700
gnomAD v4: 10-16824795-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824795C>T , CM000672.2:g.16824795C>T GRCh38
NC_000010.10:g.16866794C>T , CM000672.1:g.16866794C>T GRCh37
NC_000010.9:g.16906800C>T NCBI36
NG_008967.1:g.310023G>A , LRG_540:g.310023G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*180G>A MANE Select ENSP00000367064.4:n.*180G>A
ENST00000377833.8:c.*180G>A ENSP00000367064.4:n.*180G>A
NM_001081.3:c.*180G>A , LRG_540t1:c.*180G>A NP_001072.2:n.*180G>A
XM_011519709.1:c.*180G>A XP_011518011.1:n.*180G>A
XM_011519710.1:c.*180G>A XP_011518012.1:n.*180G>A
XM_011519711.1:c.*180G>A XP_011518013.1:n.*180G>A
XM_011519709.2:c.*180G>A XP_011518011.1:n.*180G>A
XM_011519710.2:c.*180G>A XP_011518012.1:n.*180G>A
XM_011519711.3:c.*180G>A XP_011518013.1:n.*180G>A
NM_001081.4:c.*180G>A MANE Select NP_001072.2:n.*180G>A
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