Canonical Allele Identifier: CA1893309745
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824804G= , CM000672.2:g.16824804G= GRCh38
NC_000010.10:g.16866803G= , CM000672.1:g.16866803G= GRCh37
NC_000010.9:g.16906809G= NCBI36
NG_008967.1:g.310014C= , LRG_540:g.310014C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*171C= MANE Select ENSP00000367064.4:n.*171C=
ENST00000377833.8:c.*171C= ENSP00000367064.4:n.*171C=
NM_001081.3:c.*171C= , LRG_540t1:c.*171C= NP_001072.2:n.*171C=
XM_011519709.1:c.*171C= XP_011518011.1:n.*171C=
XM_011519710.1:c.*171C= XP_011518012.1:n.*171C=
XM_011519711.1:c.*171C= XP_011518013.1:n.*171C=
XM_011519709.2:c.*171C= XP_011518011.1:n.*171C=
XM_011519710.2:c.*171C= XP_011518012.1:n.*171C=
XM_011519711.3:c.*171C= XP_011518013.1:n.*171C=
NM_001081.4:c.*171C= MANE Select NP_001072.2:n.*171C=