Canonical Allele Identifier: CA5424011

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16940183A>G , CM000672.2:g.16940183A>G	GRCh38
NC_000010.10:g.16982182A>G , CM000672.1:g.16982182A>G	GRCh37
NC_000010.9:g.17022188A>G	NCBI36
NG_008967.1:g.194635T>C , LRG_540:g.194635T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.5397T>C MANE Select	NP_001072.2:p.Arg1799=
ENST00000377833.10:c.5397T>C MANE Select	ENSP00000367064.4:p.Arg1799=
NM_001081.3:c.5397T>C , LRG_540t1:c.5397T>C	NP_001072.2:p.Arg1799=
ENST00000377833.8:c.5397T>C	ENSP00000367064.4:p.Arg1799=
XM_011519708.1:c.5397T>C	XP_011518010.1:p.Arg1799=
XM_011519708.2:c.5397T>C	XP_011518010.1:p.Arg1799=
XM_011519709.1:c.1383T>C	XP_011518011.1:p.Arg461=
XM_011519709.2:c.1383T>C	XP_011518011.1:p.Arg461=
XM_011519710.1:c.1359T>C	XP_011518012.1:p.Arg453=
XM_011519710.2:c.1359T>C	XP_011518012.1:p.Arg453=
XM_011519711.1:c.1239T>C	XP_011518013.1:p.Arg413=
XM_011519711.3:c.1239T>C	XP_011518013.1:p.Arg413=