Canonical Allele Identifier: CA2799793500

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76996270_76996271insACA , CM000675.2:g.76996270_76996271insACA	GRCh38
NC_000013.10:g.77570405_77570406insACA , CM000675.1:g.77570405_77570406insACA	GRCh37
NC_000013.9:g.76468406_76468407insACA	NCBI36
NG_009064.1:g.9347_9348insACA , LRG_692:g.9347_9348insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.565+143_565+144insACA (CLN5) MANE Select	ENSP00000366673.5:n.565+143_565+144insACA
ENST00000485938.4:c.*132_*133insACA (CLN5)	ENSP00000482959.3:n.*132_*133insACA
ENST00000616833.6:c.565+143_565+144insACA (CLN5)	ENSP00000479547.3:n.565+143_565+144insACA
ENST00000635838.1:c.174+143_174+144insACA
ENST00000635905.1:n.566+143_566+144insACA (CLN5)
ENST00000635915.1:c.563+143_563+144insACA (CLN5)
ENST00000636183.2:c.565+143_565+144insACA (CLN5)	ENSP00000490181.2:n.565+143_565+144insACA
ENST00000636520.1:n.2220_2221insACA (CLN5)
ENST00000636525.2:c.565+143_565+144insACA (CLN5)	ENSP00000490078.2:n.565+143_565+144insACA
ENST00000636602.1:n.654_655insACA (CLN5)
ENST00000636681.1:c.*256+143_*256+144insACA (CLN5)	ENSP00000489922.1:n.*256+143_*256+144insACA
ENST00000636705.1:c.401+143_401+144insACA (CLN5)
ENST00000636767.2:c.565+143_565+144insACA (CLN5)	ENSP00000489855.2:n.565+143_565+144insACA
ENST00000636780.2:c.565+143_565+144insACA (CLN5)	ENSP00000489809.2:n.565+143_565+144insACA
ENST00000637192.1:c.213+143_213+144insACA
ENST00000637278.1:n.891+143_891+144insACA (CLN5)
ENST00000637397.2:c.565+143_565+144insACA (CLN5)	ENSP00000490422.2:n.565+143_565+144insACA
ENST00000637537.2:c.565+143_565+144insACA (CLN5)	ENSP00000489711.2:n.565+143_565+144insACA
ENST00000638101.1:c.169+143_169+144insACA	ENSP00000490535.1:n.169+143_169+144insACA
ENST00000638147.2:c.565+143_565+144insACA	ENSP00000490953.2:n.565+143_565+144insACA
ENST00000377453.7:c.712+143_712+144insACA (CLN5)	ENSP00000366673.3:n.712+143_712+144insACA
ENST00000485797.2:n.174-3320_174-3319insTGT (FBXL3)
ENST00000485938.2:c.691_692insACA (CLN5)
ENST00000616833.4:c.565+143_565+144insACA (CLN5)	ENSP00000479547.1:n.565+143_565+144insACA
NM_006493.2:c.712+143_712+144insACA , LRG_692t1:c.712+143_712+144insACA (CLN5)	NP_006484.1:n.712+143_712+144insACA
XM_011534917.1:c.712+143_712+144insACA (CLN5)	XP_011533219.1:n.712+143_712+144insACA
NM_001366624.1:c.565+143_565+144insACA (CLN5)	NP_001353553.1:n.565+143_565+144insACA
NM_006493.3:c.565+143_565+144insACA (CLN5)	NP_006484.2:n.565+143_565+144insACA
XM_017020538.2:c.644-3320_644-3319insTGT (FBXL3)	XP_016876027.1:n.644-3320_644-3319insTGT
NM_001366624.2:c.565+143_565+144insACA (CLN5)	NP_001353553.1:n.565+143_565+144insACA
NM_006493.4:c.565+143_565+144insACA (CLN5) MANE Select	NP_006484.2:n.565+143_565+144insACA