Canonical Allele Identifier: CA1893472757

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129762T= , CM000672.2:g.17129762T=	GRCh38
NC_000010.10:g.17171761T= , CM000672.1:g.17171761T=	GRCh37
NC_000010.9:g.17211767T=	NCBI36
NG_008967.1:g.5056A= , LRG_540:g.5056A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.4A= MANE Select	ENSP00000367064.4:p.Met2=
ENST00000377823.1:c.4A=	ENSP00000367054.1:p.Met2=
ENST00000377833.8:c.4A=	ENSP00000367064.4:p.Met2=
NM_001081.3:c.4A= , LRG_540t1:c.4A=	NP_001072.2:p.Met2=
XM_011519708.1:c.4A=	XP_011518010.1:p.Met2=
XM_011519708.2:c.4A=	XP_011518010.1:p.Met2=
NM_001081.4:c.4A= MANE Select	NP_001072.2:p.Met2=