Canonical Allele Identifier: CA925381812

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828727_16828735dup , CM000672.2:g.16828727_16828735dup	GRCh38
NC_000010.10:g.16870726_16870734dup , CM000672.1:g.16870726_16870734dup	GRCh37
NC_000010.9:g.16910732_16910740dup	NCBI36
NG_008967.1:g.306087_306095dup , LRG_540:g.306087_306095dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10764+74_10764+82dup MANE Select	ENSP00000367064.4:n.10764+74_10764+82dup
ENST00000377833.8:c.10764+74_10764+82dup	ENSP00000367064.4:n.10764+74_10764+82dup
NM_001081.3:c.10764+74_10764+82dup , LRG_540t1:c.10764+74_10764+82dup	NP_001072.2:n.10764+74_10764+82dup
XM_011519709.1:c.6750+74_6750+82dup	XP_011518011.1:n.6750+74_6750+82dup
XM_011519710.1:c.6726+74_6726+82dup	XP_011518012.1:n.6726+74_6726+82dup
XM_011519711.1:c.6606+74_6606+82dup	XP_011518013.1:n.6606+74_6606+82dup
XM_011519709.2:c.6750+74_6750+82dup	XP_011518011.1:n.6750+74_6750+82dup
XM_011519710.2:c.6726+74_6726+82dup	XP_011518012.1:n.6726+74_6726+82dup
XM_011519711.3:c.6606+74_6606+82dup	XP_011518013.1:n.6606+74_6606+82dup
NM_001081.4:c.10764+74_10764+82dup MANE Select	NP_001072.2:n.10764+74_10764+82dup