Canonical Allele Identifier: CA1893309762
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824818G= , CM000672.2:g.16824818G= GRCh38
NC_000010.10:g.16866817G= , CM000672.1:g.16866817G= GRCh37
NC_000010.9:g.16906823G= NCBI36
NG_008967.1:g.310000C= , LRG_540:g.310000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*157C= MANE Select ENSP00000367064.4:n.*157C=
ENST00000377833.8:c.*157C= ENSP00000367064.4:n.*157C=
NM_001081.3:c.*157C= , LRG_540t1:c.*157C= NP_001072.2:n.*157C=
XM_011519709.1:c.*157C= XP_011518011.1:n.*157C=
XM_011519710.1:c.*157C= XP_011518012.1:n.*157C=
XM_011519711.1:c.*157C= XP_011518013.1:n.*157C=
XM_011519709.2:c.*157C= XP_011518011.1:n.*157C=
XM_011519710.2:c.*157C= XP_011518012.1:n.*157C=
XM_011519711.3:c.*157C= XP_011518013.1:n.*157C=
NM_001081.4:c.*157C= MANE Select NP_001072.2:n.*157C=