Canonical Allele Identifier: CA12726487

Gene: UBXN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58411603G>A , CM000670.2:g.58411603G>A	GRCh38
NC_000008.10:g.59324162G>A , CM000670.1:g.59324162G>A	GRCh37
NC_000008.9:g.59486716G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399598.7:c.84+134G>A MANE Select	ENSP00000382507.2:n.84+134G>A
ENST00000399598.6:c.84+134G>A	ENSP00000382507.2:n.84+134G>A
ENST00000520732.5:c.84+134G>A	ENSP00000427759.1:n.84+134G>A
ENST00000522978.1:n.111+134G>A
ENST00000523409.5:c.84+134G>A	ENSP00000428314.1:n.84+134G>A
NM_001077619.1:c.84+134G>A	NP_001071087.1:n.84+134G>A
XM_005251165.1:c.84+134G>A	XP_005251222.1:n.84+134G>A
XM_005251166.1:c.84+134G>A	XP_005251223.1:n.84+134G>A
XR_242453.1:n.109+134G>A
NM_001330535.1:c.84+134G>A	NP_001317464.1:n.84+134G>A
NM_001363181.1:c.84+134G>A	NP_001350110.1:n.84+134G>A
NR_156456.1:n.109+134G>A
NM_001077619.2:c.84+134G>A MANE Select	NP_001071087.1:n.84+134G>A
NM_001330535.2:c.84+134G>A	NP_001317464.1:n.84+134G>A