Canonical Allele Identifier: CA2608404885

Gene: CUBN

Linked Data

• gnomAD v4: 10-17126611-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17126611G>A , CM000672.2:g.17126611G>A	GRCh38
NC_000010.10:g.17168610G>A , CM000672.1:g.17168610G>A	GRCh37
NC_000010.9:g.17208616G>A	NCBI36
NG_008967.1:g.8207C>T , LRG_540:g.8207C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.387+150C>T MANE Select	ENSP00000367064.4:n.387+150C>T
ENST00000377823.1:c.387+150C>T	ENSP00000367054.1:n.387+150C>T
ENST00000377833.8:c.387+150C>T	ENSP00000367064.4:n.387+150C>T
ENST00000433666.5:c.48+150C>T	ENSP00000415970.1:n.48+150C>T
NM_001081.3:c.387+150C>T , LRG_540t1:c.387+150C>T	NP_001072.2:n.387+150C>T
XM_011519708.1:c.387+150C>T	XP_011518010.1:n.387+150C>T
XM_011519708.2:c.387+150C>T	XP_011518010.1:n.387+150C>T
NM_001081.4:c.387+150C>T MANE Select	NP_001072.2:n.387+150C>T