Canonical Allele Identifier: CA376127061
Community Standard Title: NM_001081.4(CUBN):c.9435G>T (p.Met3145Ile)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16869655C>A , CM000672.2:g.16869655C>A GRCh38
NC_000010.10:g.16911654C>A , CM000672.1:g.16911654C>A GRCh37
NC_000010.9:g.16951660C>A NCBI36
NG_008967.1:g.265163G>T , LRG_540:g.265163G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.9435G>T MANE Select NP_001072.2:p.Met3145Ile
ENST00000377833.10:c.9435G>T MANE Select ENSP00000367064.4:p.Met3145Ile
NM_001081.3:c.9435G>T , LRG_540t1:c.9435G>T NP_001072.2:p.Met3145Ile
ENST00000377833.8:c.9435G>T ENSP00000367064.4:p.Met3145Ile
XM_011519709.1:c.5421G>T XP_011518011.1:p.Met1807Ile
XM_011519709.2:c.5421G>T XP_011518011.1:p.Met1807Ile
XM_011519710.1:c.5397G>T XP_011518012.1:p.Met1799Ile
XM_011519710.2:c.5397G>T XP_011518012.1:p.Met1799Ile
XM_011519711.1:c.5277G>T XP_011518013.1:p.Met1759Ile
XM_011519711.3:c.5277G>T XP_011518013.1:p.Met1759Ile