Canonical Allele Identifier: CA2103428279

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76996051T= , CM000675.2:g.76996051T=	GRCh38
NC_000013.10:g.77570186T= , CM000675.1:g.77570186T=	GRCh37
NC_000013.9:g.76468187T=	NCBI36
NG_009064.1:g.9128T= , LRG_692:g.9128T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.489T= (CLN5) MANE Select	ENSP00000366673.5:p.Ala163=
ENST00000485938.4:c.489T= (CLN5)	ENSP00000482959.3:p.Ala163=
ENST00000616833.6:c.489T= (CLN5)	ENSP00000479547.3:p.Ala163=
ENST00000635838.1:c.98T=
ENST00000635905.1:n.490T= (CLN5)
ENST00000635915.1:c.487T= (CLN5)
ENST00000635989.1:n.556T= (CLN5)
ENST00000636183.2:c.489T= (CLN5)	ENSP00000490181.2:p.Ala163=
ENST00000636520.1:n.2001T= (CLN5)
ENST00000636525.2:c.489T= (CLN5)	ENSP00000490078.2:p.Ala163=
ENST00000636602.1:n.435T= (CLN5)
ENST00000636681.1:c.*180T= (CLN5)	ENSP00000489922.1:n.*180T=
ENST00000636705.1:c.325T= (CLN5)
ENST00000636767.2:c.489T= (CLN5)	ENSP00000489855.2:p.Ala163=
ENST00000636780.2:c.489T= (CLN5)	ENSP00000489809.2:p.Ala163=
ENST00000637192.1:c.137T=
ENST00000637278.1:n.815T= (CLN5)
ENST00000637397.2:c.489T= (CLN5)	ENSP00000490422.2:p.Ala163=
ENST00000637537.2:c.489T= (CLN5)	ENSP00000489711.2:p.Ala163=
ENST00000638101.1:c.93T=	ENSP00000490535.1:p.Ala31=
ENST00000638147.2:c.489T=	ENSP00000490953.2:p.Ala163=
ENST00000377453.7:c.636T= (CLN5)	ENSP00000366673.3:p.Ala212=
ENST00000485797.2:n.174-3100A= (FBXL3)
ENST00000485938.2:c.472T= (CLN5)
ENST00000616833.4:c.489T= (CLN5)	ENSP00000479547.1:p.Ala163=
NM_006493.2:c.636T= , LRG_692t1:c.636T= (CLN5)	NP_006484.1:p.Ala212=
XM_011534917.1:c.636T= (CLN5)	XP_011533219.1:p.Ala212=
NM_001366624.1:c.489T= (CLN5)	NP_001353553.1:p.Ala163=
NM_006493.3:c.489T= (CLN5)	NP_006484.2:p.Ala163=
XM_017020538.2:c.644-3100A= (FBXL3)	XP_016876027.1:n.644-3100A=
NM_001366624.2:c.489T= (CLN5)	NP_001353553.1:p.Ala163=
NM_006493.4:c.489T= (CLN5) MANE Select	NP_006484.2:p.Ala163=