Canonical Allele Identifier: CA376145999

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957836C>A (hg19) ; chr10:g.16915837C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915837C>A , CM000672.2:g.16915837C>A	GRCh38
NC_000010.10:g.16957836C>A , CM000672.1:g.16957836C>A	GRCh37
NC_000010.9:g.16997842C>A	NCBI36
NG_008967.1:g.218981G>T , LRG_540:g.218981G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7194G>T MANE Select	ENSP00000367064.4:p.Trp2398Cys
ENST00000377833.8:c.7194G>T	ENSP00000367064.4:p.Trp2398Cys
NM_001081.3:c.7194G>T , LRG_540t1:c.7194G>T	NP_001072.2:p.Trp2398Cys
XM_011519708.1:c.7194G>T	XP_011518010.1:p.Trp2398Cys
XM_011519709.1:c.3180G>T	XP_011518011.1:p.Trp1060Cys
XM_011519710.1:c.3156G>T	XP_011518012.1:p.Trp1052Cys
XM_011519711.1:c.3036G>T	XP_011518013.1:p.Trp1012Cys
XM_011519708.2:c.7194G>T	XP_011518010.1:p.Trp2398Cys
XM_011519709.2:c.3180G>T	XP_011518011.1:p.Trp1060Cys
XM_011519710.2:c.3156G>T	XP_011518012.1:p.Trp1052Cys
XM_011519711.3:c.3036G>T	XP_011518013.1:p.Trp1012Cys
NM_001081.4:c.7194G>T MANE Select	NP_001072.2:p.Trp2398Cys