Canonical Allele Identifier: CA468301759

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957962T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915963T>A , CM000672.2:g.16915963T>A	GRCh38
NC_000010.10:g.16957962T>A , CM000672.1:g.16957962T>A	GRCh37
NC_000010.9:g.16997968T>A	NCBI36
NG_008967.1:g.218855A>T , LRG_540:g.218855A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7068A>T MANE Select	ENSP00000367064.4:p.Pro2356=
ENST00000377833.8:c.7068A>T	ENSP00000367064.4:p.Pro2356=
NM_001081.3:c.7068A>T , LRG_540t1:c.7068A>T	NP_001072.2:p.Pro2356=
XM_011519708.1:c.7068A>T	XP_011518010.1:p.Pro2356=
XM_011519709.1:c.3054A>T	XP_011518011.1:p.Pro1018=
XM_011519710.1:c.3030A>T	XP_011518012.1:p.Pro1010=
XM_011519711.1:c.2910A>T	XP_011518013.1:p.Pro970=
XM_011519708.2:c.7068A>T	XP_011518010.1:p.Pro2356=
XM_011519709.2:c.3054A>T	XP_011518011.1:p.Pro1018=
XM_011519710.2:c.3030A>T	XP_011518012.1:p.Pro1010=
XM_011519711.3:c.2910A>T	XP_011518013.1:p.Pro970=
NM_001081.4:c.7068A>T MANE Select	NP_001072.2:p.Pro2356=