Canonical Allele Identifier: CA376123407

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16840360C>A , CM000672.2:g.16840360C>A	GRCh38
NC_000010.10:g.16882359C>A , CM000672.1:g.16882359C>A	GRCh37
NC_000010.9:g.16922365C>A	NCBI36
NG_008967.1:g.294458G>T , LRG_540:g.294458G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10002G>T MANE Select	NP_001072.2:p.Gln3334His
ENST00000377833.10:c.10002G>T MANE Select	ENSP00000367064.4:p.Gln3334His
NM_001081.3:c.10002G>T , LRG_540t1:c.10002G>T	NP_001072.2:p.Gln3334His
ENST00000377833.8:c.10002G>T	ENSP00000367064.4:p.Gln3334His
XM_011519709.1:c.5988G>T	XP_011518011.1:p.Gln1996His
XM_011519709.2:c.5988G>T	XP_011518011.1:p.Gln1996His
XM_011519710.1:c.5964G>T	XP_011518012.1:p.Gln1988His
XM_011519710.2:c.5964G>T	XP_011518012.1:p.Gln1988His
XM_011519711.1:c.5844G>T	XP_011518013.1:p.Gln1948His
XM_011519711.3:c.5844G>T	XP_011518013.1:p.Gln1948His