Canonical Allele Identifier: CA5422781
Community Standard Title: NM_001081.4(CUBN):c.9229G>A (p.Glu3077Lys)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16874381C>T , CM000672.2:g.16874381C>T GRCh38
NC_000010.10:g.16916380C>T , CM000672.1:g.16916380C>T GRCh37
NC_000010.9:g.16956386C>T NCBI36
NG_008967.1:g.260437G>A , LRG_540:g.260437G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.9229G>A MANE Select NP_001072.2:p.Glu3077Lys
ENST00000377833.10:c.9229G>A MANE Select ENSP00000367064.4:p.Glu3077Lys
NM_001081.3:c.9229G>A , LRG_540t1:c.9229G>A NP_001072.2:p.Glu3077Lys
ENST00000377833.8:c.9229G>A ENSP00000367064.4:p.Glu3077Lys
XM_011519709.1:c.5215G>A XP_011518011.1:p.Glu1739Lys
XM_011519709.2:c.5215G>A XP_011518011.1:p.Glu1739Lys
XM_011519710.1:c.5191G>A XP_011518012.1:p.Glu1731Lys
XM_011519710.2:c.5191G>A XP_011518012.1:p.Glu1731Lys
XM_011519711.1:c.5071G>A XP_011518013.1:p.Glu1691Lys
XM_011519711.3:c.5071G>A XP_011518013.1:p.Glu1691Lys