Canonical Allele Identifier: CA376154229
Gene: CUBN HGNC NCBI

Linked Data

COSMIC: COSM1316357
MyVariant Identifiers: chr10:g.17107536A>G (hg19) chr10:g.17065537A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065537A>G , CM000672.2:g.17065537A>G GRCh38
NC_000010.10:g.17107536A>G , CM000672.1:g.17107536A>G GRCh37
NC_000010.9:g.17147542A>G NCBI36
NG_008967.1:g.69281T>C , LRG_540:g.69281T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.3110T>C MANE Select ENSP00000367064.4:p.Ile1037Thr
ENST00000377833.8:c.3110T>C ENSP00000367064.4:p.Ile1037Thr
NM_001081.3:c.3110T>C , LRG_540t1:c.3110T>C NP_001072.2:p.Ile1037Thr
XM_011519708.1:c.3110T>C XP_011518010.1:p.Ile1037Thr
XM_011519708.2:c.3110T>C XP_011518010.1:p.Ile1037Thr
NM_001081.4:c.3110T>C MANE Select NP_001072.2:p.Ile1037Thr
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