Canonical Allele Identifier: CA5423017
Community Standard Title: NM_001081.4(CUBN):c.8463G>A (p.Trp2821Ter)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16899131C>T , CM000672.2:g.16899131C>T GRCh38
NC_000010.10:g.16941130C>T , CM000672.1:g.16941130C>T GRCh37
NC_000010.9:g.16981136C>T NCBI36
NG_008967.1:g.235687G>A , LRG_540:g.235687G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.8463G>A MANE Select NP_001072.2:p.Trp2821Ter
ENST00000377833.10:c.8463G>A MANE Select ENSP00000367064.4:p.Trp2821Ter
NM_001081.3:c.8463G>A , LRG_540t1:c.8463G>A NP_001072.2:p.Trp2821Ter
ENST00000377833.8:c.8463G>A ENSP00000367064.4:p.Trp2821Ter
XM_011519708.1:c.8463G>A XP_011518010.1:p.Trp2821Ter
XM_011519708.2:c.8463G>A XP_011518010.1:p.Trp2821Ter
XM_011519709.1:c.4449G>A XP_011518011.1:p.Trp1483Ter
XM_011519709.2:c.4449G>A XP_011518011.1:p.Trp1483Ter
XM_011519710.1:c.4425G>A XP_011518012.1:p.Trp1475Ter
XM_011519710.2:c.4425G>A XP_011518012.1:p.Trp1475Ter
XM_011519711.1:c.4305G>A XP_011518013.1:p.Trp1435Ter
XM_011519711.3:c.4305G>A XP_011518013.1:p.Trp1435Ter