Canonical Allele Identifier: CA376169051
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17126761C>A , CM000672.2:g.17126761C>A GRCh38
NC_000010.10:g.17168760C>A , CM000672.1:g.17168760C>A GRCh37
NC_000010.9:g.17208766C>A NCBI36
NG_008967.1:g.8057G>T , LRG_540:g.8057G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.387G>T MANE Select ENSP00000367064.4:p.Gln129His
ENST00000377823.1:c.387G>T ENSP00000367054.1:p.Gln129His
ENST00000377833.8:c.387G>T ENSP00000367064.4:p.Gln129His
ENST00000433666.5:c.48G>T ENSP00000415970.1:p.Gln16His
NM_001081.3:c.387G>T , LRG_540t1:c.387G>T NP_001072.2:p.Gln129His
XM_011519708.1:c.387G>T XP_011518010.1:p.Gln129His
XM_011519708.2:c.387G>T XP_011518010.1:p.Gln129His
NM_001081.4:c.387G>T MANE Select NP_001072.2:p.Gln129His