Canonical Allele Identifier: CA5422333

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828957C>A , CM000672.2:g.16828957C>A	GRCh38
NC_000010.10:g.16870956C>A , CM000672.1:g.16870956C>A	GRCh37
NC_000010.9:g.16910962C>A	NCBI36
NG_008967.1:g.305861G>T , LRG_540:g.305861G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10612G>T MANE Select	NP_001072.2:p.Glu3538Ter
ENST00000377833.10:c.10612G>T MANE Select	ENSP00000367064.4:p.Glu3538Ter
NM_001081.3:c.10612G>T , LRG_540t1:c.10612G>T	NP_001072.2:p.Glu3538Ter
ENST00000377833.8:c.10612G>T	ENSP00000367064.4:p.Glu3538Ter
XM_011519709.1:c.6598G>T	XP_011518011.1:p.Glu2200Ter
XM_011519709.2:c.6598G>T	XP_011518011.1:p.Glu2200Ter
XM_011519710.1:c.6574G>T	XP_011518012.1:p.Glu2192Ter
XM_011519710.2:c.6574G>T	XP_011518012.1:p.Glu2192Ter
XM_011519711.1:c.6454G>T	XP_011518013.1:p.Glu2152Ter
XM_011519711.3:c.6454G>T	XP_011518013.1:p.Glu2152Ter