Canonical Allele Identifier: CA376119762
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828818G>A , CM000672.2:g.16828818G>A GRCh38
NC_000010.10:g.16870817G>A , CM000672.1:g.16870817G>A GRCh37
NC_000010.9:g.16910823G>A NCBI36
NG_008967.1:g.306000C>T , LRG_540:g.306000C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10751C>T MANE Select ENSP00000367064.4:p.Pro3584Leu
ENST00000377833.8:c.10751C>T ENSP00000367064.4:p.Pro3584Leu
NM_001081.3:c.10751C>T , LRG_540t1:c.10751C>T NP_001072.2:p.Pro3584Leu
XM_011519709.1:c.6737C>T XP_011518011.1:p.Pro2246Leu
XM_011519710.1:c.6713C>T XP_011518012.1:p.Pro2238Leu
XM_011519711.1:c.6593C>T XP_011518013.1:p.Pro2198Leu
XM_011519709.2:c.6737C>T XP_011518011.1:p.Pro2246Leu
XM_011519710.2:c.6713C>T XP_011518012.1:p.Pro2238Leu
XM_011519711.3:c.6593C>T XP_011518013.1:p.Pro2198Leu
NM_001081.4:c.10751C>T MANE Select NP_001072.2:p.Pro3584Leu