Canonical Allele Identifier: CA5422545
Community Standard Title: NM_001081.4(CUBN):c.9922T>C (p.Trp3308Arg)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16840440A>G , CM000672.2:g.16840440A>G GRCh38
NC_000010.10:g.16882439A>G , CM000672.1:g.16882439A>G GRCh37
NC_000010.9:g.16922445A>G NCBI36
NG_008967.1:g.294378T>C , LRG_540:g.294378T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.9922T>C MANE Select NP_001072.2:p.Trp3308Arg
ENST00000377833.10:c.9922T>C MANE Select ENSP00000367064.4:p.Trp3308Arg
NM_001081.3:c.9922T>C , LRG_540t1:c.9922T>C NP_001072.2:p.Trp3308Arg
ENST00000377833.8:c.9922T>C ENSP00000367064.4:p.Trp3308Arg
ENST00000649135.1:n.517T>C
XM_011519709.1:c.5908T>C XP_011518011.1:p.Trp1970Arg
XM_011519709.2:c.5908T>C XP_011518011.1:p.Trp1970Arg
XM_011519710.1:c.5884T>C XP_011518012.1:p.Trp1962Arg
XM_011519710.2:c.5884T>C XP_011518012.1:p.Trp1962Arg
XM_011519711.1:c.5764T>C XP_011518013.1:p.Trp1922Arg
XM_011519711.3:c.5764T>C XP_011518013.1:p.Trp1922Arg