Canonical Allele Identifier: CA376119809
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828830G>T , CM000672.2:g.16828830G>T GRCh38
NC_000010.10:g.16870829G>T , CM000672.1:g.16870829G>T GRCh37
NC_000010.9:g.16910835G>T NCBI36
NG_008967.1:g.305988C>A , LRG_540:g.305988C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10739C>A MANE Select ENSP00000367064.4:p.Pro3580Gln
ENST00000377833.8:c.10739C>A ENSP00000367064.4:p.Pro3580Gln
NM_001081.3:c.10739C>A , LRG_540t1:c.10739C>A NP_001072.2:p.Pro3580Gln
XM_011519709.1:c.6725C>A XP_011518011.1:p.Pro2242Gln
XM_011519710.1:c.6701C>A XP_011518012.1:p.Pro2234Gln
XM_011519711.1:c.6581C>A XP_011518013.1:p.Pro2194Gln
XM_011519709.2:c.6725C>A XP_011518011.1:p.Pro2242Gln
XM_011519710.2:c.6701C>A XP_011518012.1:p.Pro2234Gln
XM_011519711.3:c.6581C>A XP_011518013.1:p.Pro2194Gln
NM_001081.4:c.10739C>A MANE Select NP_001072.2:p.Pro3580Gln