Canonical Allele Identifier: CA376118555

Gene: CUBN

Linked Data

• gnomAD v4: 10-16824989-T-A
• MyVariant Identifiers: chr10:g.16866988T>A (hg19) ; chr10:g.16824989T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824989T>A , CM000672.2:g.16824989T>A	GRCh38
NC_000010.10:g.16866988T>A , CM000672.1:g.16866988T>A	GRCh37
NC_000010.9:g.16906994T>A	NCBI36
NG_008967.1:g.309829A>T , LRG_540:g.309829A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10858A>T MANE Select	ENSP00000367064.4:p.Thr3620Ser
ENST00000377833.8:c.10858A>T	ENSP00000367064.4:p.Thr3620Ser
NM_001081.3:c.10858A>T , LRG_540t1:c.10858A>T	NP_001072.2:p.Thr3620Ser
XM_011519709.1:c.6844A>T	XP_011518011.1:p.Thr2282Ser
XM_011519710.1:c.6820A>T	XP_011518012.1:p.Thr2274Ser
XM_011519711.1:c.6700A>T	XP_011518013.1:p.Thr2234Ser
XM_011519709.2:c.6844A>T	XP_011518011.1:p.Thr2282Ser
XM_011519710.2:c.6820A>T	XP_011518012.1:p.Thr2274Ser
XM_011519711.3:c.6700A>T	XP_011518013.1:p.Thr2234Ser
NM_001081.4:c.10858A>T MANE Select	NP_001072.2:p.Thr3620Ser