Canonical Allele Identifier: CA376146216

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957873T>A (hg19) ; chr10:g.16915874T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915874T>A , CM000672.2:g.16915874T>A	GRCh38
NC_000010.10:g.16957873T>A , CM000672.1:g.16957873T>A	GRCh37
NC_000010.9:g.16997879T>A	NCBI36
NG_008967.1:g.218944A>T , LRG_540:g.218944A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.7157A>T MANE Select	ENSP00000367064.4:p.Asn2386Ile
ENST00000377833.8:c.7157A>T	ENSP00000367064.4:p.Asn2386Ile
NM_001081.3:c.7157A>T , LRG_540t1:c.7157A>T	NP_001072.2:p.Asn2386Ile
XM_011519708.1:c.7157A>T	XP_011518010.1:p.Asn2386Ile
XM_011519709.1:c.3143A>T	XP_011518011.1:p.Asn1048Ile
XM_011519710.1:c.3119A>T	XP_011518012.1:p.Asn1040Ile
XM_011519711.1:c.2999A>T	XP_011518013.1:p.Asn1000Ile
XM_011519708.2:c.7157A>T	XP_011518010.1:p.Asn2386Ile
XM_011519709.2:c.3143A>T	XP_011518011.1:p.Asn1048Ile
XM_011519710.2:c.3119A>T	XP_011518012.1:p.Asn1040Ile
XM_011519711.3:c.2999A>T	XP_011518013.1:p.Asn1000Ile
NM_001081.4:c.7157A>T MANE Select	NP_001072.2:p.Asn2386Ile