Canonical Allele Identifier: CA376118679

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16867023G>A (hg19) ; chr10:g.16825024G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825024G>A , CM000672.2:g.16825024G>A	GRCh38
NC_000010.10:g.16867023G>A , CM000672.1:g.16867023G>A	GRCh37
NC_000010.9:g.16907029G>A	NCBI36
NG_008967.1:g.309794C>T , LRG_540:g.309794C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10823C>T MANE Select	ENSP00000367064.4:p.Ala3608Val
ENST00000377833.8:c.10823C>T	ENSP00000367064.4:p.Ala3608Val
NM_001081.3:c.10823C>T , LRG_540t1:c.10823C>T	NP_001072.2:p.Ala3608Val
XM_011519709.1:c.6809C>T	XP_011518011.1:p.Ala2270Val
XM_011519710.1:c.6785C>T	XP_011518012.1:p.Ala2262Val
XM_011519711.1:c.6665C>T	XP_011518013.1:p.Ala2222Val
XM_011519709.2:c.6809C>T	XP_011518011.1:p.Ala2270Val
XM_011519710.2:c.6785C>T	XP_011518012.1:p.Ala2262Val
XM_011519711.3:c.6665C>T	XP_011518013.1:p.Ala2222Val
NM_001081.4:c.10823C>T MANE Select	NP_001072.2:p.Ala3608Val