Canonical Allele Identifier: CA1893472776
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129803C= , CM000672.2:g.17129803C= GRCh38
NC_000010.10:g.17171802C= , CM000672.1:g.17171802C= GRCh37
NC_000010.9:g.17211808C= NCBI36
NG_008967.1:g.5015G= , LRG_540:g.5015G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.-38G= MANE Select ENSP00000367064.4:n.-38G=
ENST00000377823.1:c.-38G= ENSP00000367054.1:n.-38G=
ENST00000377833.8:c.-38G= ENSP00000367064.4:n.-38G=
NM_001081.3:c.-38G= , LRG_540t1:c.-38G= NP_001072.2:n.-38G=
XM_011519708.1:c.-38G= XP_011518010.1:n.-38G=
XM_011519708.2:c.-38G= XP_011518010.1:n.-38G=
NM_001081.4:c.-38G= MANE Select NP_001072.2:n.-38G=