Canonical Allele Identifier: CA376142526

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17019959C>A , CM000672.2:g.17019959C>A	GRCh38
NC_000010.10:g.17061958C>A , CM000672.1:g.17061958C>A	GRCh37
NC_000010.9:g.17101964C>A	NCBI36
NG_008967.1:g.114859G>T , LRG_540:g.114859G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4042G>T MANE Select	NP_001072.2:p.Gly1348Ter
ENST00000377833.10:c.4042G>T MANE Select	ENSP00000367064.4:p.Gly1348Ter
NM_001081.3:c.4042G>T , LRG_540t1:c.4042G>T	NP_001072.2:p.Gly1348Ter
ENST00000377833.8:c.4042G>T	ENSP00000367064.4:p.Gly1348Ter
XM_011519708.1:c.4042G>T	XP_011518010.1:p.Gly1348Ter
XM_011519708.2:c.4042G>T	XP_011518010.1:p.Gly1348Ter
XM_011519709.1:c.28G>T	XP_011518011.1:p.Gly10Ter
XM_011519709.2:c.28G>T	XP_011518011.1:p.Gly10Ter
XM_011519710.1:c.4G>T	XP_011518012.1:p.Gly2Ter
XM_011519710.2:c.4G>T	XP_011518012.1:p.Gly2Ter