Canonical Allele Identifier: CA468407423
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.16870819T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828820T>A , CM000672.2:g.16828820T>A GRCh38
NC_000010.10:g.16870819T>A , CM000672.1:g.16870819T>A GRCh37
NC_000010.9:g.16910825T>A NCBI36
NG_008967.1:g.305998A>T , LRG_540:g.305998A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10749A>T MANE Select ENSP00000367064.4:p.Gly3583=
ENST00000377833.8:c.10749A>T ENSP00000367064.4:p.Gly3583=
NM_001081.3:c.10749A>T , LRG_540t1:c.10749A>T NP_001072.2:p.Gly3583=
XM_011519709.1:c.6735A>T XP_011518011.1:p.Gly2245=
XM_011519710.1:c.6711A>T XP_011518012.1:p.Gly2237=
XM_011519711.1:c.6591A>T XP_011518013.1:p.Gly2197=
XM_011519709.2:c.6735A>T XP_011518011.1:p.Gly2245=
XM_011519710.2:c.6711A>T XP_011518012.1:p.Gly2237=
XM_011519711.3:c.6591A>T XP_011518013.1:p.Gly2197=
NM_001081.4:c.10749A>T MANE Select NP_001072.2:p.Gly3583=