Canonical Allele Identifier: CA376146011

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957837C>T (hg19) ; chr10:g.16915838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915838C>T , CM000672.2:g.16915838C>T	GRCh38
NC_000010.10:g.16957837C>T , CM000672.1:g.16957837C>T	GRCh37
NC_000010.9:g.16997843C>T	NCBI36
NG_008967.1:g.218980G>A , LRG_540:g.218980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7193G>A MANE Select	ENSP00000367064.4:p.Trp2398Ter
ENST00000377833.8:c.7193G>A	ENSP00000367064.4:p.Trp2398Ter
NM_001081.3:c.7193G>A , LRG_540t1:c.7193G>A	NP_001072.2:p.Trp2398Ter
XM_011519708.1:c.7193G>A	XP_011518010.1:p.Trp2398Ter
XM_011519709.1:c.3179G>A	XP_011518011.1:p.Trp1060Ter
XM_011519710.1:c.3155G>A	XP_011518012.1:p.Trp1052Ter
XM_011519711.1:c.3035G>A	XP_011518013.1:p.Trp1012Ter
XM_011519708.2:c.7193G>A	XP_011518010.1:p.Trp2398Ter
XM_011519709.2:c.3179G>A	XP_011518011.1:p.Trp1060Ter
XM_011519710.2:c.3155G>A	XP_011518012.1:p.Trp1052Ter
XM_011519711.3:c.3035G>A	XP_011518013.1:p.Trp1012Ter
NM_001081.4:c.7193G>A MANE Select	NP_001072.2:p.Trp2398Ter