Canonical Allele Identifier: CA1893308815
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824014G= , CM000672.2:g.16824014G= GRCh38
NC_000010.10:g.16866013G= , CM000672.1:g.16866013G= GRCh37
NC_000010.9:g.16906019G= NCBI36
NG_008967.1:g.310804C= , LRG_540:g.310804C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*961C= MANE Select ENSP00000367064.4:n.*961C=
ENST00000377833.8:c.*961C= ENSP00000367064.4:n.*961C=
NM_001081.3:c.*961C= , LRG_540t1:c.*961C= NP_001072.2:n.*961C=
XM_011519709.1:c.*961C= XP_011518011.1:n.*961C=
XM_011519710.1:c.*961C= XP_011518012.1:n.*961C=
XM_011519711.1:c.*961C= XP_011518013.1:n.*961C=
NM_001081.4:c.*961C= MANE Select NP_001072.2:n.*961C=