Canonical Allele Identifier: CA468301672

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957860A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915861A>G , CM000672.2:g.16915861A>G	GRCh38
NC_000010.10:g.16957860A>G , CM000672.1:g.16957860A>G	GRCh37
NC_000010.9:g.16997866A>G	NCBI36
NG_008967.1:g.218957T>C , LRG_540:g.218957T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7170T>C MANE Select	ENSP00000367064.4:p.Cys2390=
ENST00000377833.8:c.7170T>C	ENSP00000367064.4:p.Cys2390=
NM_001081.3:c.7170T>C , LRG_540t1:c.7170T>C	NP_001072.2:p.Cys2390=
XM_011519708.1:c.7170T>C	XP_011518010.1:p.Cys2390=
XM_011519709.1:c.3156T>C	XP_011518011.1:p.Cys1052=
XM_011519710.1:c.3132T>C	XP_011518012.1:p.Cys1044=
XM_011519711.1:c.3012T>C	XP_011518013.1:p.Cys1004=
XM_011519708.2:c.7170T>C	XP_011518010.1:p.Cys2390=
XM_011519709.2:c.3156T>C	XP_011518011.1:p.Cys1052=
XM_011519710.2:c.3132T>C	XP_011518012.1:p.Cys1044=
XM_011519711.3:c.3012T>C	XP_011518013.1:p.Cys1004=
NM_001081.4:c.7170T>C MANE Select	NP_001072.2:p.Cys2390=