Canonical Allele Identifier: CA10917432

Gene: UBXN11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26295105G>A , CM000663.2:g.26295105G>A	GRCh38
NC_000001.10:g.26621596G>A , CM000663.1:g.26621596G>A	GRCh37
NC_000001.9:g.26494183G>A	NCBI36
NG_028986.1:g.28161C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374217.7:c.334-774C>T	ENSP00000363334.2:n.334-774C>T
ENST00000374222.6:c.433-774C>T MANE Select	ENSP00000363339.1:n.433-774C>T
ENST00000450041.6:c.208-774C>T	ENSP00000413448.2:n.208-774C>T
ENST00000314675.11:c.199+5821C>T	ENSP00000324721.7:n.199+5821C>T
ENST00000357089.8:c.334-774C>T	ENSP00000349601.4:n.334-774C>T
ENST00000374215.5:c.319-774C>T	ENSP00000363332.1:n.319-774C>T
ENST00000374217.6:c.334-774C>T	ENSP00000363334.2:n.334-774C>T
ENST00000374221.7:c.433-774C>T	ENSP00000363338.3:n.433-774C>T
ENST00000374222.5:c.433-774C>T	ENSP00000363339.1:n.433-774C>T
ENST00000374223.5:c.-171+1814C>T	ENSP00000363340.1:n.-171+1814C>T
ENST00000423664.5:c.319-774C>T	ENSP00000394036.1:n.319-774C>T
ENST00000442942.6:c.334-774C>T	ENSP00000404956.2:n.334-774C>T
ENST00000450041.5:c.208-774C>T	ENSP00000413448.1:n.208-774C>T
ENST00000452980.5:c.334-774C>T	ENSP00000410357.1:n.334-774C>T
ENST00000472155.5:n.517-774C>T
ENST00000475591.5:n.414-774C>T
ENST00000494942.5:n.199-774C>T
ENST00000496466.1:n.198-774C>T
NM_001077262.1:c.199+5821C>T	NP_001070730.1:n.199+5821C>T
NM_145345.2:c.334-774C>T	NP_663320.2:n.334-774C>T
NM_183008.2:c.433-774C>T	NP_892120.2:n.433-774C>T
NM_001077262.2:c.199+5821C>T	NP_001070730.1:n.199+5821C>T
NM_001389556.1:c.433-774C>T MANE Select	NP_001376485.1:n.433-774C>T
NM_001389559.1:c.334-774C>T	NP_001376488.1:n.334-774C>T
NM_145345.3:c.334-774C>T	NP_663320.2:n.334-774C>T
NM_183008.3:c.433-774C>T	NP_892120.2:n.433-774C>T