Canonical Allele Identifier: CA376146620

Gene: CUBN

Linked Data

• ClinVar Variation Id: 1318728
• ClinVar RCV Id: RCV001768352
• dbSNP Id: rs2131458198
• MyVariant Identifiers: chr10:g.16957942C>G (hg19) ; chr10:g.16915943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915943C>G , CM000672.2:g.16915943C>G	GRCh38
NC_000010.10:g.16957942C>G , CM000672.1:g.16957942C>G	GRCh37
NC_000010.9:g.16997948C>G	NCBI36
NG_008967.1:g.218875G>C , LRG_540:g.218875G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7088G>C MANE Select	ENSP00000367064.4:p.Cys2363Ser
ENST00000377833.8:c.7088G>C	ENSP00000367064.4:p.Cys2363Ser
NM_001081.3:c.7088G>C , LRG_540t1:c.7088G>C	NP_001072.2:p.Cys2363Ser
XM_011519708.1:c.7088G>C	XP_011518010.1:p.Cys2363Ser
XM_011519709.1:c.3074G>C	XP_011518011.1:p.Cys1025Ser
XM_011519710.1:c.3050G>C	XP_011518012.1:p.Cys1017Ser
XM_011519711.1:c.2930G>C	XP_011518013.1:p.Cys977Ser
XM_011519708.2:c.7088G>C	XP_011518010.1:p.Cys2363Ser
XM_011519709.2:c.3074G>C	XP_011518011.1:p.Cys1025Ser
XM_011519710.2:c.3050G>C	XP_011518012.1:p.Cys1017Ser
XM_011519711.3:c.2930G>C	XP_011518013.1:p.Cys977Ser
NM_001081.4:c.7088G>C MANE Select	NP_001072.2:p.Cys2363Ser