Canonical Allele Identifier: CA2103435603

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000652A= , CM000675.2:g.77000652A=	GRCh38
NC_000013.10:g.77574787A= , CM000675.1:g.77574787A=	GRCh37
NC_000013.9:g.76472788A=	NCBI36
NG_009064.1:g.13729A= , LRG_692:g.13729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.760A= (CLN5) MANE Select	ENSP00000366673.5:p.Thr254=
ENST00000616833.6:c.*202A= (CLN5)	ENSP00000479547.3:n.*202A=
ENST00000635838.1:c.174+4525A=
ENST00000635905.1:n.566+4525A= (CLN5)
ENST00000635915.1:c.758A= (CLN5)
ENST00000636183.2:c.760A= (CLN5)	ENSP00000490181.2:p.Thr254=
ENST00000636525.2:c.565+4525A= (CLN5)	ENSP00000490078.2:n.565+4525A=
ENST00000636681.1:c.*451A= (CLN5)	ENSP00000489922.1:n.*451A=
ENST00000636705.1:c.596A= (CLN5)
ENST00000636767.2:c.565+4525A= (CLN5)	ENSP00000489855.2:n.565+4525A=
ENST00000636780.2:c.*209A= (CLN5)	ENSP00000489809.2:n.*209A=
ENST00000637192.1:c.213+4525A=
ENST00000637278.1:n.1086A= (CLN5)
ENST00000637397.2:c.565+4525A= (CLN5)	ENSP00000490422.2:n.565+4525A=
ENST00000638101.1:c.169+4525A=	ENSP00000490535.1:n.169+4525A=
ENST00000638147.2:c.565+4525A=	ENSP00000490953.2:n.565+4525A=
ENST00000377453.7:c.907A= (CLN5)	ENSP00000366673.3:p.Thr303=
ENST00000477982.2:n.1657T= (FBXL3)
ENST00000485797.2:n.174-7701T= (FBXL3)
ENST00000616833.4:c.760A= (CLN5)	ENSP00000479547.1:p.Thr254=
NM_006493.2:c.907A= , LRG_692t1:c.907A= (CLN5)	NP_006484.1:p.Thr303=
XM_011534917.1:c.*209A= (CLN5)	XP_011533219.1:n.*209A=
NM_001366624.1:c.*209A= (CLN5)	NP_001353553.1:n.*209A=
NM_006493.3:c.760A= (CLN5)	NP_006484.2:p.Thr254=
XM_017020538.2:c.644-7701T= (FBXL3)	XP_016876027.1:n.644-7701T=
NM_001366624.2:c.*209A= (CLN5)	NP_001353553.1:n.*209A=
NM_006493.4:c.760A= (CLN5) MANE Select	NP_006484.2:p.Thr254=