Canonical Allele Identifier: CA5422733

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16869755A>G , CM000672.2:g.16869755A>G	GRCh38
NC_000010.10:g.16911754A>G , CM000672.1:g.16911754A>G	GRCh37
NC_000010.9:g.16951760A>G	NCBI36
NG_008967.1:g.265063T>C , LRG_540:g.265063T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9335T>C MANE Select	NP_001072.2:p.Phe3112Ser
ENST00000377833.10:c.9335T>C MANE Select	ENSP00000367064.4:p.Phe3112Ser
NM_001081.3:c.9335T>C , LRG_540t1:c.9335T>C	NP_001072.2:p.Phe3112Ser
ENST00000377833.8:c.9335T>C	ENSP00000367064.4:p.Phe3112Ser
XM_011519709.1:c.5321T>C	XP_011518011.1:p.Phe1774Ser
XM_011519709.2:c.5321T>C	XP_011518011.1:p.Phe1774Ser
XM_011519710.1:c.5297T>C	XP_011518012.1:p.Phe1766Ser
XM_011519710.2:c.5297T>C	XP_011518012.1:p.Phe1766Ser
XM_011519711.1:c.5177T>C	XP_011518013.1:p.Phe1726Ser
XM_011519711.3:c.5177T>C	XP_011518013.1:p.Phe1726Ser