Canonical Allele Identifier: CA1893471285
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17126744A= , CM000672.2:g.17126744A= GRCh38
NC_000010.10:g.17168743A= , CM000672.1:g.17168743A= GRCh37
NC_000010.9:g.17208749A= NCBI36
NG_008967.1:g.8074T= , LRG_540:g.8074T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.387+17T= MANE Select ENSP00000367064.4:n.387+17T=
ENST00000377823.1:c.387+17T= ENSP00000367054.1:n.387+17T=
ENST00000377833.8:c.387+17T= ENSP00000367064.4:n.387+17T=
ENST00000433666.5:c.48+17T= ENSP00000415970.1:n.48+17T=
NM_001081.3:c.387+17T= , LRG_540t1:c.387+17T= NP_001072.2:n.387+17T=
XM_011519708.1:c.387+17T= XP_011518010.1:n.387+17T=
XM_011519708.2:c.387+17T= XP_011518010.1:n.387+17T=
NM_001081.4:c.387+17T= MANE Select NP_001072.2:n.387+17T=