Canonical Allele Identifier: CA468301767

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957968T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915969T>G , CM000672.2:g.16915969T>G	GRCh38
NC_000010.10:g.16957968T>G , CM000672.1:g.16957968T>G	GRCh37
NC_000010.9:g.16997974T>G	NCBI36
NG_008967.1:g.218849A>C , LRG_540:g.218849A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7062A>C MANE Select	ENSP00000367064.4:p.Thr2354=
ENST00000377833.8:c.7062A>C	ENSP00000367064.4:p.Thr2354=
NM_001081.3:c.7062A>C , LRG_540t1:c.7062A>C	NP_001072.2:p.Thr2354=
XM_011519708.1:c.7062A>C	XP_011518010.1:p.Thr2354=
XM_011519709.1:c.3048A>C	XP_011518011.1:p.Thr1016=
XM_011519710.1:c.3024A>C	XP_011518012.1:p.Thr1008=
XM_011519711.1:c.2904A>C	XP_011518013.1:p.Thr968=
XM_011519708.2:c.7062A>C	XP_011518010.1:p.Thr2354=
XM_011519709.2:c.3048A>C	XP_011518011.1:p.Thr1016=
XM_011519710.2:c.3024A>C	XP_011518012.1:p.Thr1008=
XM_011519711.3:c.2904A>C	XP_011518013.1:p.Thr968=
NM_001081.4:c.7062A>C MANE Select	NP_001072.2:p.Thr2354=