Canonical Allele Identifier: CA376142712

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16904073G>T , CM000672.2:g.16904073G>T	GRCh38
NC_000010.10:g.16946072G>T , CM000672.1:g.16946072G>T	GRCh37
NC_000010.9:g.16986078G>T	NCBI36
NG_008967.1:g.230745C>A , LRG_540:g.230745C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.7955C>A MANE Select	NP_001072.2:p.Ser2652Ter
ENST00000377833.10:c.7955C>A MANE Select	ENSP00000367064.4:p.Ser2652Ter
NM_001081.3:c.7955C>A , LRG_540t1:c.7955C>A	NP_001072.2:p.Ser2652Ter
ENST00000377833.8:c.7955C>A	ENSP00000367064.4:p.Ser2652Ter
ENST00000648092.1:n.491C>A
ENST00000649933.1:n.317C>A
XM_011519708.1:c.7955C>A	XP_011518010.1:p.Ser2652Ter
XM_011519708.2:c.7955C>A	XP_011518010.1:p.Ser2652Ter
XM_011519709.1:c.3941C>A	XP_011518011.1:p.Ser1314Ter
XM_011519709.2:c.3941C>A	XP_011518011.1:p.Ser1314Ter
XM_011519710.1:c.3917C>A	XP_011518012.1:p.Ser1306Ter
XM_011519710.2:c.3917C>A	XP_011518012.1:p.Ser1306Ter
XM_011519711.1:c.3797C>A	XP_011518013.1:p.Ser1266Ter
XM_011519711.3:c.3797C>A	XP_011518013.1:p.Ser1266Ter