Canonical Allele Identifier: CA1893472750

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129752G= , CM000672.2:g.17129752G=	GRCh38
NC_000010.10:g.17171751G= , CM000672.1:g.17171751G=	GRCh37
NC_000010.9:g.17211757G=	NCBI36
NG_008967.1:g.5066C= , LRG_540:g.5066C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.14C= MANE Select	ENSP00000367064.4:p.Ser5=
ENST00000377823.1:c.14C=	ENSP00000367054.1:p.Ser5=
ENST00000377833.8:c.14C=	ENSP00000367064.4:p.Ser5=
NM_001081.3:c.14C= , LRG_540t1:c.14C=	NP_001072.2:p.Ser5=
XM_011519708.1:c.14C=	XP_011518010.1:p.Ser5=
XM_011519708.2:c.14C=	XP_011518010.1:p.Ser5=
NM_001081.4:c.14C= MANE Select	NP_001072.2:p.Ser5=