Canonical Allele Identifier: CA468407519

Gene: CUBN

Linked Data

• dbSNP Id: rs1835737152
• gnomAD v3: 10-17071438-T-A
• gnomAD v4: 10-17071438-T-A
• MyVariant Identifiers: chr10:g.17113437T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17071438T>A , CM000672.2:g.17071438T>A	GRCh38
NC_000010.10:g.17113437T>A , CM000672.1:g.17113437T>A	GRCh37
NC_000010.9:g.17153443T>A	NCBI36
NG_008967.1:g.63380A>T , LRG_540:g.63380A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.2613A>T MANE Select	ENSP00000367064.4:p.Thr871=
ENST00000377833.8:c.2613A>T	ENSP00000367064.4:p.Thr871=
NM_001081.3:c.2613A>T , LRG_540t1:c.2613A>T	NP_001072.2:p.Thr871=
XM_011519708.1:c.2613A>T	XP_011518010.1:p.Thr871=
XM_011519708.2:c.2613A>T	XP_011518010.1:p.Thr871=
NM_001081.4:c.2613A>T MANE Select	NP_001072.2:p.Thr871=