Canonical Allele Identifier: CA203550585

Gene: CUBN

Linked Data

• dbSNP Id: rs1009390422
• gnomAD v3: 10-16955776-G-A
• gnomAD v4: 10-16955776-G-A
• MyVariant Identifiers: chr10:g.16997775G>A (hg19) ; chr10:g.16955776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16955776G>A , CM000672.2:g.16955776G>A	GRCh38
NC_000010.10:g.16997775G>A , CM000672.1:g.16997775G>A	GRCh37
NC_000010.9:g.17037781G>A	NCBI36
NG_008967.1:g.179042C>T , LRG_540:g.179042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.4696-1228C>T MANE Select	ENSP00000367064.4:n.4696-1228C>T
ENST00000377833.8:c.4696-1228C>T	ENSP00000367064.4:n.4696-1228C>T
NM_001081.3:c.4696-1228C>T , LRG_540t1:c.4696-1228C>T	NP_001072.2:n.4696-1228C>T
XM_011519708.1:c.4696-1228C>T	XP_011518010.1:n.4696-1228C>T
XM_011519709.1:c.682-1228C>T	XP_011518011.1:n.682-1228C>T
XM_011519710.1:c.658-1228C>T	XP_011518012.1:n.658-1228C>T
XM_011519711.1:c.538-1228C>T	XP_011518013.1:n.538-1228C>T
XM_011519708.2:c.4696-1228C>T	XP_011518010.1:n.4696-1228C>T
XM_011519709.2:c.682-1228C>T	XP_011518011.1:n.682-1228C>T
XM_011519710.2:c.658-1228C>T	XP_011518012.1:n.658-1228C>T
XM_011519711.3:c.538-1228C>T	XP_011518013.1:n.538-1228C>T
NM_001081.4:c.4696-1228C>T MANE Select	NP_001072.2:n.4696-1228C>T