Canonical Allele Identifier: CA2103428173

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76996013C= , CM000675.2:g.76996013C=	GRCh38
NC_000013.10:g.77570148C= , CM000675.1:g.77570148C=	GRCh37
NC_000013.9:g.76468149C=	NCBI36
NG_009064.1:g.9090C= , LRG_692:g.9090C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.451C= (CLN5) MANE Select	ENSP00000366673.5:p.Pro151=
ENST00000485938.4:c.451C= (CLN5)	ENSP00000482959.3:p.Pro151=
ENST00000616833.6:c.451C= (CLN5)	ENSP00000479547.3:p.Pro151=
ENST00000635838.1:c.60C=
ENST00000635905.1:n.452C= (CLN5)
ENST00000635915.1:c.449C= (CLN5)
ENST00000635989.1:n.518C= (CLN5)
ENST00000636183.2:c.451C= (CLN5)	ENSP00000490181.2:p.Pro151=
ENST00000636520.1:n.1963C= (CLN5)
ENST00000636525.2:c.451C= (CLN5)	ENSP00000490078.2:p.Pro151=
ENST00000636602.1:n.397C= (CLN5)
ENST00000636681.1:c.*142C= (CLN5)	ENSP00000489922.1:n.*142C=
ENST00000636705.1:c.287C= (CLN5)
ENST00000636767.2:c.451C= (CLN5)	ENSP00000489855.2:p.Pro151=
ENST00000636780.2:c.451C= (CLN5)	ENSP00000489809.2:p.Pro151=
ENST00000637192.1:c.99C=
ENST00000637278.1:n.777C= (CLN5)
ENST00000637397.2:c.451C= (CLN5)	ENSP00000490422.2:p.Pro151=
ENST00000637537.2:c.451C= (CLN5)	ENSP00000489711.2:p.Pro151=
ENST00000638101.1:c.55C=	ENSP00000490535.1:p.Pro19=
ENST00000638147.2:c.451C=	ENSP00000490953.2:p.Pro151=
ENST00000377453.7:c.598C= (CLN5)	ENSP00000366673.3:p.Pro200=
ENST00000485797.2:n.174-3062G= (FBXL3)
ENST00000485938.2:c.434C= (CLN5)
ENST00000616833.4:c.451C= (CLN5)	ENSP00000479547.1:p.Pro151=
NM_006493.2:c.598C= , LRG_692t1:c.598C= (CLN5)	NP_006484.1:p.Pro200=
XM_011534917.1:c.598C= (CLN5)	XP_011533219.1:p.Pro200=
NM_001366624.1:c.451C= (CLN5)	NP_001353553.1:p.Pro151=
NM_006493.3:c.451C= (CLN5)	NP_006484.2:p.Pro151=
XM_017020538.2:c.644-3062G= (FBXL3)	XP_016876027.1:n.644-3062G=
NM_001366624.2:c.451C= (CLN5)	NP_001353553.1:p.Pro151=
NM_006493.4:c.451C= (CLN5) MANE Select	NP_006484.2:p.Pro151=