Canonical Allele Identifier: CA1893442192
Gene: CUBN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065409C= , CM000672.2:g.17065409C= GRCh38
NC_000010.10:g.17107408C= , CM000672.1:g.17107408C= GRCh37
NC_000010.9:g.17147414C= NCBI36
NG_008967.1:g.69409G= , LRG_540:g.69409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3139+99G= MANE Select ENSP00000367064.4:n.3139+99G=
ENST00000377833.8:c.3139+99G= ENSP00000367064.4:n.3139+99G=
NM_001081.3:c.3139+99G= , LRG_540t1:c.3139+99G= NP_001072.2:n.3139+99G=
XM_011519708.1:c.3139+99G= XP_011518010.1:n.3139+99G=
XM_011519708.2:c.3139+99G= XP_011518010.1:n.3139+99G=
NM_001081.4:c.3139+99G= MANE Select NP_001072.2:n.3139+99G=
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