Canonical Allele Identifier: CA592157716

Gene: CUBN

Linked Data

• dbSNP Id: rs1357416800
• gnomAD v2: 10-17171775-G-A
• MyVariant Identifiers: chr10:g.17171775G>A (hg19) ; chr10:g.17129776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129776G>A , CM000672.2:g.17129776G>A	GRCh38
NC_000010.10:g.17171775G>A , CM000672.1:g.17171775G>A	GRCh37
NC_000010.9:g.17211781G>A	NCBI36
NG_008967.1:g.5042C>T , LRG_540:g.5042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.-11C>T MANE Select	ENSP00000367064.4:n.-11C>T
ENST00000377823.1:c.-11C>T	ENSP00000367054.1:n.-11C>T
ENST00000377833.8:c.-11C>T	ENSP00000367064.4:n.-11C>T
NM_001081.3:c.-11C>T , LRG_540t1:c.-11C>T	NP_001072.2:n.-11C>T
XM_011519708.1:c.-11C>T	XP_011518010.1:n.-11C>T
XM_011519708.2:c.-11C>T	XP_011518010.1:n.-11C>T
NM_001081.4:c.-11C>T MANE Select	NP_001072.2:n.-11C>T