Canonical Allele Identifier: CA5424061

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16947273G>A , CM000672.2:g.16947273G>A	GRCh38
NC_000010.10:g.16989272G>A , CM000672.1:g.16989272G>A	GRCh37
NC_000010.9:g.17029278G>A	NCBI36
NG_008967.1:g.187545C>T , LRG_540:g.187545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.5304C>T MANE Select	ENSP00000367064.4:p.Ile1768=
ENST00000377833.8:c.5304C>T	ENSP00000367064.4:p.Ile1768=
NM_001081.3:c.5304C>T , LRG_540t1:c.5304C>T	NP_001072.2:p.Ile1768=
XM_011519708.1:c.5304C>T	XP_011518010.1:p.Ile1768=
XM_011519709.1:c.1290C>T	XP_011518011.1:p.Ile430=
XM_011519710.1:c.1266C>T	XP_011518012.1:p.Ile422=
XM_011519711.1:c.1146C>T	XP_011518013.1:p.Ile382=
XM_011519708.2:c.5304C>T	XP_011518010.1:p.Ile1768=
XM_011519709.2:c.1290C>T	XP_011518011.1:p.Ile430=
XM_011519710.2:c.1266C>T	XP_011518012.1:p.Ile422=
XM_011519711.3:c.1146C>T	XP_011518013.1:p.Ile382=
NM_001081.4:c.5304C>T MANE Select	NP_001072.2:p.Ile1768=