Canonical Allele Identifier: CA376170164
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17171762C>T (hg19) chr10:g.17129763C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129763C>T , CM000672.2:g.17129763C>T GRCh38
NC_000010.10:g.17171762C>T , CM000672.1:g.17171762C>T GRCh37
NC_000010.9:g.17211768C>T NCBI36
NG_008967.1:g.5055G>A , LRG_540:g.5055G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.3G>A MANE Select ENSP00000367064.4:p.Met1Ile
ENST00000377823.1:c.3G>A ENSP00000367054.1:p.Met1Ile
ENST00000377833.8:c.3G>A ENSP00000367064.4:p.Met1Ile
NM_001081.3:c.3G>A , LRG_540t1:c.3G>A NP_001072.2:p.Met1Ile
XM_011519708.1:c.3G>A XP_011518010.1:p.Met1Ile
XM_011519708.2:c.3G>A XP_011518010.1:p.Met1Ile
NM_001081.4:c.3G>A MANE Select NP_001072.2:p.Met1Ile
Search 100 bp 5'
Search 100 bp 3'