Canonical Allele Identifier: CA1893309862
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824914C= , CM000672.2:g.16824914C= GRCh38
NC_000010.10:g.16866913C= , CM000672.1:g.16866913C= GRCh37
NC_000010.9:g.16906919C= NCBI36
NG_008967.1:g.309904G= , LRG_540:g.309904G=

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*61G= MANE Select ENSP00000367064.4:n.*61G=
ENST00000377833.8:c.*61G= ENSP00000367064.4:n.*61G=
NM_001081.3:c.*61G= , LRG_540t1:c.*61G= NP_001072.2:n.*61G=
XM_011519709.1:c.*61G= XP_011518011.1:n.*61G=
XM_011519710.1:c.*61G= XP_011518012.1:n.*61G=
XM_011519711.1:c.*61G= XP_011518013.1:n.*61G=
XM_011519709.2:c.*61G= XP_011518011.1:n.*61G=
XM_011519710.2:c.*61G= XP_011518012.1:n.*61G=
XM_011519711.3:c.*61G= XP_011518013.1:n.*61G=
NM_001081.4:c.*61G= MANE Select NP_001072.2:n.*61G=