Canonical Allele Identifier: CA376170155

Gene: CUBN

Linked Data

• gnomAD v4: 10-17129760-C-A
• MyVariant Identifiers: chr10:g.17171759C>A (hg19) ; chr10:g.17129760C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129760C>A , CM000672.2:g.17129760C>A	GRCh38
NC_000010.10:g.17171759C>A , CM000672.1:g.17171759C>A	GRCh37
NC_000010.9:g.17211765C>A	NCBI36
NG_008967.1:g.5058G>T , LRG_540:g.5058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.6G>T MANE Select	ENSP00000367064.4:p.Met2Ile
ENST00000377823.1:c.6G>T	ENSP00000367054.1:p.Met2Ile
ENST00000377833.8:c.6G>T	ENSP00000367064.4:p.Met2Ile
NM_001081.3:c.6G>T , LRG_540t1:c.6G>T	NP_001072.2:p.Met2Ile
XM_011519708.1:c.6G>T	XP_011518010.1:p.Met2Ile
XM_011519708.2:c.6G>T	XP_011518010.1:p.Met2Ile
NM_001081.4:c.6G>T MANE Select	NP_001072.2:p.Met2Ile