Canonical Allele Identifier: CA2608395668
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824104C>A , CM000672.2:g.16824104C>A GRCh38
NC_000010.10:g.16866103C>A , CM000672.1:g.16866103C>A GRCh37
NC_000010.9:g.16906109C>A NCBI36
NG_008967.1:g.310714G>T , LRG_540:g.310714G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*871G>T MANE Select ENSP00000367064.4:n.*871G>T
ENST00000377833.8:c.*871G>T ENSP00000367064.4:n.*871G>T
NM_001081.3:c.*871G>T , LRG_540t1:c.*871G>T NP_001072.2:n.*871G>T
XM_011519709.1:c.*871G>T XP_011518011.1:n.*871G>T
XM_011519710.1:c.*871G>T XP_011518012.1:n.*871G>T
XM_011519711.1:c.*871G>T XP_011518013.1:n.*871G>T
NM_001081.4:c.*871G>T MANE Select NP_001072.2:n.*871G>T