Canonical Allele Identifier: CA2103428155

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76996010C= , CM000675.2:g.76996010C=	GRCh38
NC_000013.10:g.77570145C= , CM000675.1:g.77570145C=	GRCh37
NC_000013.9:g.76468146C=	NCBI36
NG_009064.1:g.9087C= , LRG_692:g.9087C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.448C= (CLN5) MANE Select	ENSP00000366673.5:p.Arg150=
ENST00000485938.4:c.448C= (CLN5)	ENSP00000482959.3:p.Arg150=
ENST00000616833.6:c.448C= (CLN5)	ENSP00000479547.3:p.Arg150=
ENST00000635838.1:c.57C=
ENST00000635905.1:n.449C= (CLN5)
ENST00000635915.1:c.446C= (CLN5)
ENST00000635989.1:n.515C= (CLN5)
ENST00000636183.2:c.448C= (CLN5)	ENSP00000490181.2:p.Arg150=
ENST00000636520.1:n.1960C= (CLN5)
ENST00000636525.2:c.448C= (CLN5)	ENSP00000490078.2:p.Arg150=
ENST00000636602.1:n.394C= (CLN5)
ENST00000636681.1:c.*139C= (CLN5)	ENSP00000489922.1:n.*139C=
ENST00000636705.1:c.284C= (CLN5)
ENST00000636767.2:c.448C= (CLN5)	ENSP00000489855.2:p.Arg150=
ENST00000636780.2:c.448C= (CLN5)	ENSP00000489809.2:p.Arg150=
ENST00000637192.1:c.96C=
ENST00000637278.1:n.774C= (CLN5)
ENST00000637397.2:c.448C= (CLN5)	ENSP00000490422.2:p.Arg150=
ENST00000637537.2:c.448C= (CLN5)	ENSP00000489711.2:p.Arg150=
ENST00000638101.1:c.52C=	ENSP00000490535.1:p.Arg18=
ENST00000638147.2:c.448C=	ENSP00000490953.2:p.Arg150=
ENST00000377453.7:c.595C= (CLN5)	ENSP00000366673.3:p.Arg199=
ENST00000485797.2:n.174-3059G= (FBXL3)
ENST00000485938.2:c.431C= (CLN5)
ENST00000616833.4:c.448C= (CLN5)	ENSP00000479547.1:p.Arg150=
NM_006493.2:c.595C= , LRG_692t1:c.595C= (CLN5)	NP_006484.1:p.Arg199=
XM_011534917.1:c.595C= (CLN5)	XP_011533219.1:p.Arg199=
NM_001366624.1:c.448C= (CLN5)	NP_001353553.1:p.Arg150=
NM_006493.3:c.448C= (CLN5)	NP_006484.2:p.Arg150=
XM_017020538.2:c.644-3059G= (FBXL3)	XP_016876027.1:n.644-3059G=
NM_001366624.2:c.448C= (CLN5)	NP_001353553.1:p.Arg150=
NM_006493.4:c.448C= (CLN5) MANE Select	NP_006484.2:p.Arg150=