Canonical Allele Identifier: CA2608400639
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-17065454-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065454G>T , CM000672.2:g.17065454G>T GRCh38
NC_000010.10:g.17107453G>T , CM000672.1:g.17107453G>T GRCh37
NC_000010.9:g.17147459G>T NCBI36
NG_008967.1:g.69364C>A , LRG_540:g.69364C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.3139+54C>A MANE Select ENSP00000367064.4:n.3139+54C>A
ENST00000377833.8:c.3139+54C>A ENSP00000367064.4:n.3139+54C>A
NM_001081.3:c.3139+54C>A , LRG_540t1:c.3139+54C>A NP_001072.2:n.3139+54C>A
XM_011519708.1:c.3139+54C>A XP_011518010.1:n.3139+54C>A
XM_011519708.2:c.3139+54C>A XP_011518010.1:n.3139+54C>A
NM_001081.4:c.3139+54C>A MANE Select NP_001072.2:n.3139+54C>A
Search 100 bp 5'
Search 100 bp 3'