Canonical Allele Identifier: CA376118631

Gene: CUBN

Linked Data

• gnomAD v4: 10-16825007-G-T
• MyVariant Identifiers: chr10:g.16867006G>T (hg19) ; chr10:g.16825007G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825007G>T , CM000672.2:g.16825007G>T	GRCh38
NC_000010.10:g.16867006G>T , CM000672.1:g.16867006G>T	GRCh37
NC_000010.9:g.16907012G>T	NCBI36
NG_008967.1:g.309811C>A , LRG_540:g.309811C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10840C>A MANE Select	ENSP00000367064.4:p.Pro3614Thr
ENST00000377833.8:c.10840C>A	ENSP00000367064.4:p.Pro3614Thr
NM_001081.3:c.10840C>A , LRG_540t1:c.10840C>A	NP_001072.2:p.Pro3614Thr
XM_011519709.1:c.6826C>A	XP_011518011.1:p.Pro2276Thr
XM_011519710.1:c.6802C>A	XP_011518012.1:p.Pro2268Thr
XM_011519711.1:c.6682C>A	XP_011518013.1:p.Pro2228Thr
XM_011519709.2:c.6826C>A	XP_011518011.1:p.Pro2276Thr
XM_011519710.2:c.6802C>A	XP_011518012.1:p.Pro2268Thr
XM_011519711.3:c.6682C>A	XP_011518013.1:p.Pro2228Thr
NM_001081.4:c.10840C>A MANE Select	NP_001072.2:p.Pro3614Thr