Canonical Allele Identifier: CA662288808

Gene: CUBN

Linked Data

• dbSNP Id: rs1454529239
• gnomAD v3: 10-16824727-C-G
• gnomAD v4: 10-16824727-C-G
• MyVariant Identifiers: chr10:g.16866726C>G (hg19) ; chr10:g.16824727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824727C>G , CM000672.2:g.16824727C>G	GRCh38
NC_000010.10:g.16866726C>G , CM000672.1:g.16866726C>G	GRCh37
NC_000010.9:g.16906732C>G	NCBI36
NG_008967.1:g.310091G>C , LRG_540:g.310091G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*248G>C MANE Select	ENSP00000367064.4:n.*248G>C
ENST00000377833.8:c.*248G>C	ENSP00000367064.4:n.*248G>C
NM_001081.3:c.*248G>C , LRG_540t1:c.*248G>C	NP_001072.2:n.*248G>C
XM_011519709.1:c.*248G>C	XP_011518011.1:n.*248G>C
XM_011519710.1:c.*248G>C	XP_011518012.1:n.*248G>C
XM_011519711.1:c.*248G>C	XP_011518013.1:n.*248G>C
XM_011519709.2:c.*248G>C	XP_011518011.1:n.*248G>C
XM_011519710.2:c.*248G>C	XP_011518012.1:n.*248G>C
XM_011519711.3:c.*248G>C	XP_011518013.1:n.*248G>C
NM_001081.4:c.*248G>C MANE Select	NP_001072.2:n.*248G>C