Canonical Allele Identifier: CA376146671

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957951T>G (hg19) ; chr10:g.16915952T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915952T>G , CM000672.2:g.16915952T>G	GRCh38
NC_000010.10:g.16957951T>G , CM000672.1:g.16957951T>G	GRCh37
NC_000010.9:g.16997957T>G	NCBI36
NG_008967.1:g.218866A>C , LRG_540:g.218866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7079A>C MANE Select	ENSP00000367064.4:p.Asn2360Thr
ENST00000377833.8:c.7079A>C	ENSP00000367064.4:p.Asn2360Thr
NM_001081.3:c.7079A>C , LRG_540t1:c.7079A>C	NP_001072.2:p.Asn2360Thr
XM_011519708.1:c.7079A>C	XP_011518010.1:p.Asn2360Thr
XM_011519709.1:c.3065A>C	XP_011518011.1:p.Asn1022Thr
XM_011519710.1:c.3041A>C	XP_011518012.1:p.Asn1014Thr
XM_011519711.1:c.2921A>C	XP_011518013.1:p.Asn974Thr
XM_011519708.2:c.7079A>C	XP_011518010.1:p.Asn2360Thr
XM_011519709.2:c.3065A>C	XP_011518011.1:p.Asn1022Thr
XM_011519710.2:c.3041A>C	XP_011518012.1:p.Asn1014Thr
XM_011519711.3:c.2921A>C	XP_011518013.1:p.Asn974Thr
NM_001081.4:c.7079A>C MANE Select	NP_001072.2:p.Asn2360Thr