Canonical Allele Identifier: CA376169597
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17171123A>T (hg19) chr10:g.17129124A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129124A>T , CM000672.2:g.17129124A>T GRCh38
NC_000010.10:g.17171123A>T , CM000672.1:g.17171123A>T GRCh37
NC_000010.9:g.17211129A>T NCBI36
NG_008967.1:g.5694T>A , LRG_540:g.5694T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.249T>A MANE Select ENSP00000367064.4:p.His83Gln
ENST00000377823.1:c.249T>A ENSP00000367054.1:p.His83Gln
ENST00000377833.8:c.249T>A ENSP00000367064.4:p.His83Gln
NM_001081.3:c.249T>A , LRG_540t1:c.249T>A NP_001072.2:p.His83Gln
XM_011519708.1:c.249T>A XP_011518010.1:p.His83Gln
XM_011519708.2:c.249T>A XP_011518010.1:p.His83Gln
NM_001081.4:c.249T>A MANE Select NP_001072.2:p.His83Gln
Search 100 bp 5'
Search 100 bp 3'