Canonical Allele Identifier: CA2103427745

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76995892_76995894delinsCTT , CM000675.2:g.76995892_76995894delinsCTT	GRCh38
NC_000013.10:g.77570027_77570029delinsCTT , CM000675.1:g.77570027_77570029delinsCTT	GRCh37
NC_000013.9:g.76468028_76468030delinsCTT	NCBI36
NG_009064.1:g.8969_8971delinsCTT , LRG_692:g.8969_8971delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.340-10_340-8delinsCTT (CLN5) MANE Select	ENSP00000366673.5:n.340-10_340-8delinsCTT
ENST00000485938.4:c.340-10_340-8delinsCTT (CLN5)	ENSP00000482959.3:n.340-10_340-8delinsCTT
ENST00000616833.6:c.340-10_340-8delinsCTT (CLN5)	ENSP00000479547.3:n.340-10_340-8delinsCTT
ENST00000635905.1:n.341-10_341-8delinsCTT (CLN5)
ENST00000635915.1:c.328_330delinsCTT (CLN5)
ENST00000635989.1:n.407-10_407-8delinsCTT (CLN5)
ENST00000636183.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000490181.2:n.340-10_340-8delinsCTT
ENST00000636520.1:n.1842_1844delinsCTT (CLN5)
ENST00000636525.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000490078.2:n.340-10_340-8delinsCTT
ENST00000636602.1:n.286-10_286-8delinsCTT (CLN5)
ENST00000636681.1:c.*31-10_*31-8delinsCTT (CLN5)	ENSP00000489922.1:n.*31-10_*31-8delinsCTT
ENST00000636705.1:c.176-10_176-8delinsCTT (CLN5)
ENST00000636767.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000489855.2:n.340-10_340-8delinsCTT
ENST00000636780.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000489809.2:n.340-10_340-8delinsCTT
ENST00000637278.1:n.656_658delinsCTT (CLN5)
ENST00000637397.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000490422.2:n.340-10_340-8delinsCTT
ENST00000637537.2:c.340-10_340-8delinsCTT (CLN5)	ENSP00000489711.2:n.340-10_340-8delinsCTT
ENST00000638147.2:c.340-10_340-8delinsCTT	ENSP00000490953.2:n.340-10_340-8delinsCTT
ENST00000377453.7:c.487-10_487-8delinsCTT (CLN5)	ENSP00000366673.3:n.487-10_487-8delinsCTT
ENST00000485797.2:n.174-2943_174-2941delinsAAG (FBXL3)
ENST00000485938.2:c.323-10_323-8delinsCTT (CLN5)
ENST00000616833.4:c.340-10_340-8delinsCTT (CLN5)	ENSP00000479547.1:n.340-10_340-8delinsCTT
NM_006493.2:c.487-10_487-8delinsCTT , LRG_692t1:c.487-10_487-8delinsCTT (CLN5)	NP_006484.1:n.487-10_487-8delinsCTT
XM_011534917.1:c.487-10_487-8delinsCTT (CLN5)	XP_011533219.1:n.487-10_487-8delinsCTT
NM_001366624.1:c.340-10_340-8delinsCTT (CLN5)	NP_001353553.1:n.340-10_340-8delinsCTT
NM_006493.3:c.340-10_340-8delinsCTT (CLN5)	NP_006484.2:n.340-10_340-8delinsCTT
XM_017020538.2:c.644-2943_644-2941delinsAAG (FBXL3)	XP_016876027.1:n.644-2943_644-2941delinsAAG
NM_001366624.2:c.340-10_340-8delinsCTT (CLN5)	NP_001353553.1:n.340-10_340-8delinsCTT
NM_006493.4:c.340-10_340-8delinsCTT (CLN5) MANE Select	NP_006484.2:n.340-10_340-8delinsCTT