Canonical Allele Identifier: CA2539837842

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16923297C>A , CM000672.2:g.16923297C>A	GRCh38
NC_000010.10:g.16965296C>A , CM000672.1:g.16965296C>A	GRCh37
NC_000010.9:g.17005302C>A	NCBI36
NG_008967.1:g.211521G>T , LRG_540:g.211521G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.6646+1944G>T MANE Select	ENSP00000367064.4:n.6646+1944G>T
ENST00000377833.8:c.6646+1944G>T	ENSP00000367064.4:n.6646+1944G>T
NM_001081.3:c.6646+1944G>T , LRG_540t1:c.6646+1944G>T	NP_001072.2:n.6646+1944G>T
XM_011519708.1:c.6646+1944G>T	XP_011518010.1:n.6646+1944G>T
XM_011519709.1:c.2632+1944G>T	XP_011518011.1:n.2632+1944G>T
XM_011519710.1:c.2608+1944G>T	XP_011518012.1:n.2608+1944G>T
XM_011519711.1:c.2488+1944G>T	XP_011518013.1:n.2488+1944G>T
XM_011519708.2:c.6646+1944G>T	XP_011518010.1:n.6646+1944G>T
XM_011519709.2:c.2632+1944G>T	XP_011518011.1:n.2632+1944G>T
XM_011519710.2:c.2608+1944G>T	XP_011518012.1:n.2608+1944G>T
XM_011519711.3:c.2488+1944G>T	XP_011518013.1:n.2488+1944G>T
NM_001081.4:c.6646+1944G>T MANE Select	NP_001072.2:n.6646+1944G>T