Canonical Allele Identifier: CA2574521629
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-17065413-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065413A>G , CM000672.2:g.17065413A>G GRCh38
NC_000010.10:g.17107412A>G , CM000672.1:g.17107412A>G GRCh37
NC_000010.9:g.17147418A>G NCBI36
NG_008967.1:g.69405T>C , LRG_540:g.69405T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3139+95T>C MANE Select ENSP00000367064.4:n.3139+95T>C
ENST00000377833.8:c.3139+95T>C ENSP00000367064.4:n.3139+95T>C
NM_001081.3:c.3139+95T>C , LRG_540t1:c.3139+95T>C NP_001072.2:n.3139+95T>C
XM_011519708.1:c.3139+95T>C XP_011518010.1:n.3139+95T>C
XM_011519708.2:c.3139+95T>C XP_011518010.1:n.3139+95T>C
NM_001081.4:c.3139+95T>C MANE Select NP_001072.2:n.3139+95T>C
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