Canonical Allele Identifier: CA2608396175

Gene: CUBN

Linked Data

• gnomAD v4: 10-16824822-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824822T>A , CM000672.2:g.16824822T>A	GRCh38
NC_000010.10:g.16866821T>A , CM000672.1:g.16866821T>A	GRCh37
NC_000010.9:g.16906827T>A	NCBI36
NG_008967.1:g.309996A>T , LRG_540:g.309996A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*153A>T MANE Select	ENSP00000367064.4:n.*153A>T
ENST00000377833.8:c.*153A>T	ENSP00000367064.4:n.*153A>T
NM_001081.3:c.*153A>T , LRG_540t1:c.*153A>T	NP_001072.2:n.*153A>T
XM_011519709.1:c.*153A>T	XP_011518011.1:n.*153A>T
XM_011519710.1:c.*153A>T	XP_011518012.1:n.*153A>T
XM_011519711.1:c.*153A>T	XP_011518013.1:n.*153A>T
XM_011519709.2:c.*153A>T	XP_011518011.1:n.*153A>T
XM_011519710.2:c.*153A>T	XP_011518012.1:n.*153A>T
XM_011519711.3:c.*153A>T	XP_011518013.1:n.*153A>T
NM_001081.4:c.*153A>T MANE Select	NP_001072.2:n.*153A>T