Canonical Allele Identifier: CA468301682

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957869A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915870A>C , CM000672.2:g.16915870A>C	GRCh38
NC_000010.10:g.16957869A>C , CM000672.1:g.16957869A>C	GRCh37
NC_000010.9:g.16997875A>C	NCBI36
NG_008967.1:g.218948T>G , LRG_540:g.218948T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.7161T>G MANE Select	ENSP00000367064.4:p.Ser2387=
ENST00000377833.8:c.7161T>G	ENSP00000367064.4:p.Ser2387=
NM_001081.3:c.7161T>G , LRG_540t1:c.7161T>G	NP_001072.2:p.Ser2387=
XM_011519708.1:c.7161T>G	XP_011518010.1:p.Ser2387=
XM_011519709.1:c.3147T>G	XP_011518011.1:p.Ser1049=
XM_011519710.1:c.3123T>G	XP_011518012.1:p.Ser1041=
XM_011519711.1:c.3003T>G	XP_011518013.1:p.Ser1001=
XM_011519708.2:c.7161T>G	XP_011518010.1:p.Ser2387=
XM_011519709.2:c.3147T>G	XP_011518011.1:p.Ser1049=
XM_011519710.2:c.3123T>G	XP_011518012.1:p.Ser1041=
XM_011519711.3:c.3003T>G	XP_011518013.1:p.Ser1001=
NM_001081.4:c.7161T>G MANE Select	NP_001072.2:p.Ser2387=