Canonical Allele Identifier: CA2103434910

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000458G= , CM000675.2:g.77000458G=	GRCh38
NC_000013.10:g.77574593G= , CM000675.1:g.77574593G=	GRCh37
NC_000013.9:g.76472594G=	NCBI36
NG_009064.1:g.13535G= , LRG_692:g.13535G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.566G= (CLN5) MANE Select	ENSP00000366673.5:p.Gly189=
ENST00000616833.6:c.*8G= (CLN5)	ENSP00000479547.3:n.*8G=
ENST00000635838.1:c.174+4331G=
ENST00000635905.1:n.566+4331G= (CLN5)
ENST00000635915.1:c.564G= (CLN5)
ENST00000636183.2:c.566G= (CLN5)	ENSP00000490181.2:p.Gly189=
ENST00000636525.2:c.565+4331G= (CLN5)	ENSP00000490078.2:n.565+4331G=
ENST00000636681.1:c.*257G= (CLN5)	ENSP00000489922.1:n.*257G=
ENST00000636705.1:c.402G= (CLN5)
ENST00000636767.2:c.565+4331G= (CLN5)	ENSP00000489855.2:n.565+4331G=
ENST00000636780.2:c.*15G= (CLN5)	ENSP00000489809.2:n.*15G=
ENST00000637192.1:c.213+4331G=
ENST00000637278.1:n.892G= (CLN5)
ENST00000637397.2:c.565+4331G= (CLN5)	ENSP00000490422.2:n.565+4331G=
ENST00000638101.1:c.169+4331G=	ENSP00000490535.1:n.169+4331G=
ENST00000638147.2:c.565+4331G=	ENSP00000490953.2:n.565+4331G=
ENST00000377453.7:c.713G= (CLN5)	ENSP00000366673.3:p.Gly238=
ENST00000477982.2:n.1851C= (FBXL3)
ENST00000485797.2:n.174-7507C= (FBXL3)
ENST00000616833.4:c.566G= (CLN5)	ENSP00000479547.1:p.Gly189=
NM_006493.2:c.713G= , LRG_692t1:c.713G= (CLN5)	NP_006484.1:p.Gly238=
XM_011534917.1:c.*15G= (CLN5)	XP_011533219.1:n.*15G=
NM_001366624.1:c.*15G= (CLN5)	NP_001353553.1:n.*15G=
NM_006493.3:c.566G= (CLN5)	NP_006484.2:p.Gly189=
XM_017020538.2:c.644-7507C= (FBXL3)	XP_016876027.1:n.644-7507C=
NM_001366624.2:c.*15G= (CLN5)	NP_001353553.1:n.*15G=
NM_006493.4:c.566G= (CLN5) MANE Select	NP_006484.2:p.Gly189=