Canonical Allele Identifier: CA1893472724

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129693C= , CM000672.2:g.17129693C=	GRCh38
NC_000010.10:g.17171692C= , CM000672.1:g.17171692C=	GRCh37
NC_000010.9:g.17211698C=	NCBI36
NG_008967.1:g.5125G= , LRG_540:g.5125G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.73G= MANE Select	ENSP00000367064.4:p.Ala25=
ENST00000377823.1:c.73G=	ENSP00000367054.1:p.Ala25=
ENST00000377833.8:c.73G=	ENSP00000367064.4:p.Ala25=
NM_001081.3:c.73G= , LRG_540t1:c.73G=	NP_001072.2:p.Ala25=
XM_011519708.1:c.73G=	XP_011518010.1:p.Ala25=
XM_011519708.2:c.73G=	XP_011518010.1:p.Ala25=
NM_001081.4:c.73G= MANE Select	NP_001072.2:p.Ala25=