Canonical Allele Identifier: CA1893309972

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825009C= , CM000672.2:g.16825009C=	GRCh38
NC_000010.10:g.16867008C= , CM000672.1:g.16867008C=	GRCh37
NC_000010.9:g.16907014C=	NCBI36
NG_008967.1:g.309809G= , LRG_540:g.309809G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10838G= MANE Select	ENSP00000367064.4:p.Arg3613=
ENST00000377833.8:c.10838G=	ENSP00000367064.4:p.Arg3613=
NM_001081.3:c.10838G= , LRG_540t1:c.10838G=	NP_001072.2:p.Arg3613=
XM_011519709.1:c.6824G=	XP_011518011.1:p.Arg2275=
XM_011519710.1:c.6800G=	XP_011518012.1:p.Arg2267=
XM_011519711.1:c.6680G=	XP_011518013.1:p.Arg2227=
XM_011519709.2:c.6824G=	XP_011518011.1:p.Arg2275=
XM_011519710.2:c.6800G=	XP_011518012.1:p.Arg2267=
XM_011519711.3:c.6680G=	XP_011518013.1:p.Arg2227=
NM_001081.4:c.10838G= MANE Select	NP_001072.2:p.Arg3613=