Canonical Allele Identifier: CA2574500613

Gene: CUBN

Linked Data

• gnomAD v4: 10-16915723-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915723A>C , CM000672.2:g.16915723A>C	GRCh38
NC_000010.10:g.16957722A>C , CM000672.1:g.16957722A>C	GRCh37
NC_000010.9:g.16997728A>C	NCBI36
NG_008967.1:g.219095T>G , LRG_540:g.219095T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7210+98T>G MANE Select	ENSP00000367064.4:n.7210+98T>G
ENST00000377833.8:c.7210+98T>G	ENSP00000367064.4:n.7210+98T>G
NM_001081.3:c.7210+98T>G , LRG_540t1:c.7210+98T>G	NP_001072.2:n.7210+98T>G
XM_011519708.1:c.7210+98T>G	XP_011518010.1:n.7210+98T>G
XM_011519709.1:c.3196+98T>G	XP_011518011.1:n.3196+98T>G
XM_011519710.1:c.3172+98T>G	XP_011518012.1:n.3172+98T>G
XM_011519711.1:c.3052+98T>G	XP_011518013.1:n.3052+98T>G
XM_011519708.2:c.7210+98T>G	XP_011518010.1:n.7210+98T>G
XM_011519709.2:c.3196+98T>G	XP_011518011.1:n.3196+98T>G
XM_011519710.2:c.3172+98T>G	XP_011518012.1:n.3172+98T>G
XM_011519711.3:c.3052+98T>G	XP_011518013.1:n.3052+98T>G
NM_001081.4:c.7210+98T>G MANE Select	NP_001072.2:n.7210+98T>G