Canonical Allele Identifier: CA5422883

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16888428A>G , CM000672.2:g.16888428A>G	GRCh38
NC_000010.10:g.16930427A>G , CM000672.1:g.16930427A>G	GRCh37
NC_000010.9:g.16970433A>G	NCBI36
NG_008967.1:g.246390T>C , LRG_540:g.246390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.8894T>C MANE Select	ENSP00000367064.4:p.Phe2965Ser
ENST00000377833.8:c.8894T>C	ENSP00000367064.4:p.Phe2965Ser
NM_001081.3:c.8894T>C , LRG_540t1:c.8894T>C	NP_001072.2:p.Phe2965Ser
XM_011519709.1:c.4880T>C	XP_011518011.1:p.Phe1627Ser
XM_011519710.1:c.4856T>C	XP_011518012.1:p.Phe1619Ser
XM_011519711.1:c.4736T>C	XP_011518013.1:p.Phe1579Ser
XM_011519709.2:c.4880T>C	XP_011518011.1:p.Phe1627Ser
XM_011519710.2:c.4856T>C	XP_011518012.1:p.Phe1619Ser
XM_011519711.3:c.4736T>C	XP_011518013.1:p.Phe1579Ser
NM_001081.4:c.8894T>C MANE Select	NP_001072.2:p.Phe2965Ser