Canonical Allele Identifier: CA1893309612

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824717A= , CM000672.2:g.16824717A=	GRCh38
NC_000010.10:g.16866716A= , CM000672.1:g.16866716A=	GRCh37
NC_000010.9:g.16906722A=	NCBI36
NG_008967.1:g.310101T= , LRG_540:g.310101T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*258T= MANE Select	ENSP00000367064.4:n.*258T=
ENST00000377833.8:c.*258T=	ENSP00000367064.4:n.*258T=
NM_001081.3:c.*258T= , LRG_540t1:c.*258T=	NP_001072.2:n.*258T=
XM_011519709.1:c.*258T=	XP_011518011.1:n.*258T=
XM_011519710.1:c.*258T=	XP_011518012.1:n.*258T=
XM_011519711.1:c.*258T=	XP_011518013.1:n.*258T=
XM_011519709.2:c.*258T=	XP_011518011.1:n.*258T=
XM_011519710.2:c.*258T=	XP_011518012.1:n.*258T=
XM_011519711.3:c.*258T=	XP_011518013.1:n.*258T=
NM_001081.4:c.*258T= MANE Select	NP_001072.2:n.*258T=