Canonical Allele Identifier: CA5423750

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16928165A>G , CM000672.2:g.16928165A>G	GRCh38
NC_000010.10:g.16970164A>G , CM000672.1:g.16970164A>G	GRCh37
NC_000010.9:g.17010170A>G	NCBI36
NG_008967.1:g.206653T>C , LRG_540:g.206653T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.6263T>C MANE Select	ENSP00000367064.4:p.Phe2088Ser
ENST00000377833.8:c.6263T>C	ENSP00000367064.4:p.Phe2088Ser
NM_001081.3:c.6263T>C , LRG_540t1:c.6263T>C	NP_001072.2:p.Phe2088Ser
XM_011519708.1:c.6263T>C	XP_011518010.1:p.Phe2088Ser
XM_011519709.1:c.2249T>C	XP_011518011.1:p.Phe750Ser
XM_011519710.1:c.2225T>C	XP_011518012.1:p.Phe742Ser
XM_011519711.1:c.2105T>C	XP_011518013.1:p.Phe702Ser
XM_011519708.2:c.6263T>C	XP_011518010.1:p.Phe2088Ser
XM_011519709.2:c.2249T>C	XP_011518011.1:p.Phe750Ser
XM_011519710.2:c.2225T>C	XP_011518012.1:p.Phe742Ser
XM_011519711.3:c.2105T>C	XP_011518013.1:p.Phe702Ser
NM_001081.4:c.6263T>C MANE Select	NP_001072.2:p.Phe2088Ser