Canonical Allele Identifier: CA468301681

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957866A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915867A>G , CM000672.2:g.16915867A>G	GRCh38
NC_000010.10:g.16957866A>G , CM000672.1:g.16957866A>G	GRCh37
NC_000010.9:g.16997872A>G	NCBI36
NG_008967.1:g.218951T>C , LRG_540:g.218951T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.7164T>C MANE Select	ENSP00000367064.4:p.Ser2388=
ENST00000377833.8:c.7164T>C	ENSP00000367064.4:p.Ser2388=
NM_001081.3:c.7164T>C , LRG_540t1:c.7164T>C	NP_001072.2:p.Ser2388=
XM_011519708.1:c.7164T>C	XP_011518010.1:p.Ser2388=
XM_011519709.1:c.3150T>C	XP_011518011.1:p.Ser1050=
XM_011519710.1:c.3126T>C	XP_011518012.1:p.Ser1042=
XM_011519711.1:c.3006T>C	XP_011518013.1:p.Ser1002=
XM_011519708.2:c.7164T>C	XP_011518010.1:p.Ser2388=
XM_011519709.2:c.3150T>C	XP_011518011.1:p.Ser1050=
XM_011519710.2:c.3126T>C	XP_011518012.1:p.Ser1042=
XM_011519711.3:c.3006T>C	XP_011518013.1:p.Ser1002=
NM_001081.4:c.7164T>C MANE Select	NP_001072.2:p.Ser2388=