Canonical Allele Identifier: CA5422425

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16835111G>A , CM000672.2:g.16835111G>A	GRCh38
NC_000010.10:g.16877110G>A , CM000672.1:g.16877110G>A	GRCh37
NC_000010.9:g.16917116G>A	NCBI36
NG_008967.1:g.299707C>T , LRG_540:g.299707C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10265C>T MANE Select	ENSP00000367064.4:p.Thr3422Ile
ENST00000377833.8:c.10265C>T	ENSP00000367064.4:p.Thr3422Ile
NM_001081.3:c.10265C>T , LRG_540t1:c.10265C>T	NP_001072.2:p.Thr3422Ile
XM_011519709.1:c.6251C>T	XP_011518011.1:p.Thr2084Ile
XM_011519710.1:c.6227C>T	XP_011518012.1:p.Thr2076Ile
XM_011519711.1:c.6107C>T	XP_011518013.1:p.Thr2036Ile
XM_011519709.2:c.6251C>T	XP_011518011.1:p.Thr2084Ile
XM_011519710.2:c.6227C>T	XP_011518012.1:p.Thr2076Ile
XM_011519711.3:c.6107C>T	XP_011518013.1:p.Thr2036Ile
NM_001081.4:c.10265C>T MANE Select	NP_001072.2:p.Thr3422Ile