Canonical Allele Identifier: CA5422963

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16890491G>T , CM000672.2:g.16890491G>T	GRCh38
NC_000010.10:g.16932490G>T , CM000672.1:g.16932490G>T	GRCh37
NC_000010.9:g.16972496G>T	NCBI36
NG_008967.1:g.244327C>A , LRG_540:g.244327C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.8635C>A MANE Select	ENSP00000367064.4:p.Leu2879Ile
ENST00000377833.8:c.8635C>A	ENSP00000367064.4:p.Leu2879Ile
NM_001081.3:c.8635C>A , LRG_540t1:c.8635C>A	NP_001072.2:p.Leu2879Ile
XM_011519709.1:c.4621C>A	XP_011518011.1:p.Leu1541Ile
XM_011519710.1:c.4597C>A	XP_011518012.1:p.Leu1533Ile
XM_011519711.1:c.4477C>A	XP_011518013.1:p.Leu1493Ile
XM_011519709.2:c.4621C>A	XP_011518011.1:p.Leu1541Ile
XM_011519710.2:c.4597C>A	XP_011518012.1:p.Leu1533Ile
XM_011519711.3:c.4477C>A	XP_011518013.1:p.Leu1493Ile
NM_001081.4:c.8635C>A MANE Select	NP_001072.2:p.Leu2879Ile