Canonical Allele Identifier: CA376119775
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828821C>T , CM000672.2:g.16828821C>T GRCh38
NC_000010.10:g.16870820C>T , CM000672.1:g.16870820C>T GRCh37
NC_000010.9:g.16910826C>T NCBI36
NG_008967.1:g.305997G>A , LRG_540:g.305997G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10748G>A MANE Select ENSP00000367064.4:p.Gly3583Glu
ENST00000377833.8:c.10748G>A ENSP00000367064.4:p.Gly3583Glu
NM_001081.3:c.10748G>A , LRG_540t1:c.10748G>A NP_001072.2:p.Gly3583Glu
XM_011519709.1:c.6734G>A XP_011518011.1:p.Gly2245Glu
XM_011519710.1:c.6710G>A XP_011518012.1:p.Gly2237Glu
XM_011519711.1:c.6590G>A XP_011518013.1:p.Gly2197Glu
XM_011519709.2:c.6734G>A XP_011518011.1:p.Gly2245Glu
XM_011519710.2:c.6710G>A XP_011518012.1:p.Gly2237Glu
XM_011519711.3:c.6590G>A XP_011518013.1:p.Gly2197Glu
NM_001081.4:c.10748G>A MANE Select NP_001072.2:p.Gly3583Glu