Canonical Allele Identifier: CA5422793

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16874444C>T , CM000672.2:g.16874444C>T	GRCh38
NC_000010.10:g.16916443C>T , CM000672.1:g.16916443C>T	GRCh37
NC_000010.9:g.16956449C>T	NCBI36
NG_008967.1:g.260374G>A , LRG_540:g.260374G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9166G>A MANE Select	NP_001072.2:p.Ala3056Thr
ENST00000377833.10:c.9166G>A MANE Select	ENSP00000367064.4:p.Ala3056Thr
NM_001081.3:c.9166G>A , LRG_540t1:c.9166G>A	NP_001072.2:p.Ala3056Thr
ENST00000377833.8:c.9166G>A	ENSP00000367064.4:p.Ala3056Thr
XM_011519709.1:c.5152G>A	XP_011518011.1:p.Ala1718Thr
XM_011519709.2:c.5152G>A	XP_011518011.1:p.Ala1718Thr
XM_011519710.1:c.5128G>A	XP_011518012.1:p.Ala1710Thr
XM_011519710.2:c.5128G>A	XP_011518012.1:p.Ala1710Thr
XM_011519711.1:c.5008G>A	XP_011518013.1:p.Ala1670Thr
XM_011519711.3:c.5008G>A	XP_011518013.1:p.Ala1670Thr