Canonical Allele Identifier: CA203533457

Gene: CUBN

Linked Data

• dbSNP Id: rs932757613
• gnomAD v3: 10-16828732-A-T
• gnomAD v4: 10-16828732-A-T
• MyVariant Identifiers: chr10:g.16870731A>T (hg19) ; chr10:g.16828732A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828732A>T , CM000672.2:g.16828732A>T	GRCh38
NC_000010.10:g.16870731A>T , CM000672.1:g.16870731A>T	GRCh37
NC_000010.9:g.16910737A>T	NCBI36
NG_008967.1:g.306086T>A , LRG_540:g.306086T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10764+73T>A MANE Select	ENSP00000367064.4:n.10764+73T>A
ENST00000377833.8:c.10764+73T>A	ENSP00000367064.4:n.10764+73T>A
NM_001081.3:c.10764+73T>A , LRG_540t1:c.10764+73T>A	NP_001072.2:n.10764+73T>A
XM_011519709.1:c.6750+73T>A	XP_011518011.1:n.6750+73T>A
XM_011519710.1:c.6726+73T>A	XP_011518012.1:n.6726+73T>A
XM_011519711.1:c.6606+73T>A	XP_011518013.1:n.6606+73T>A
XM_011519709.2:c.6750+73T>A	XP_011518011.1:n.6750+73T>A
XM_011519710.2:c.6726+73T>A	XP_011518012.1:n.6726+73T>A
XM_011519711.3:c.6606+73T>A	XP_011518013.1:n.6606+73T>A
NM_001081.4:c.10764+73T>A MANE Select	NP_001072.2:n.10764+73T>A