Canonical Allele Identifier: CA2103437224

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77001128T= , CM000675.2:g.77001128T=	GRCh38
NC_000013.10:g.77575263T= , CM000675.1:g.77575263T=	GRCh37
NC_000013.9:g.76473264T=	NCBI36
NG_009064.1:g.14205T= , LRG_692:g.14205T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.*159T= (CLN5) MANE Select	ENSP00000366673.5:n.*159T=
ENST00000616833.6:c.*678T= (CLN5)	ENSP00000479547.3:n.*678T=
ENST00000635838.1:c.174+5001T=
ENST00000635905.1:n.566+5001T= (CLN5)
ENST00000635915.1:c.1234T= (CLN5)
ENST00000636183.2:c.*159T= (CLN5)	ENSP00000490181.2:n.*159T=
ENST00000636525.2:c.565+5001T= (CLN5)	ENSP00000490078.2:n.565+5001T=
ENST00000636681.1:c.*927T= (CLN5)	ENSP00000489922.1:n.*927T=
ENST00000636705.1:c.1072T= (CLN5)
ENST00000636767.2:c.565+5001T= (CLN5)	ENSP00000489855.2:n.565+5001T=
ENST00000636780.2:c.*685T= (CLN5)	ENSP00000489809.2:n.*685T=
ENST00000637192.1:c.213+5001T=
ENST00000637278.1:n.1562T= (CLN5)
ENST00000637397.2:c.565+5001T= (CLN5)	ENSP00000490422.2:n.565+5001T=
ENST00000638101.1:c.169+5001T=	ENSP00000490535.1:n.169+5001T=
ENST00000638147.2:c.565+5001T=	ENSP00000490953.2:n.565+5001T=
ENST00000377453.7:c.*159T= (CLN5)	ENSP00000366673.3:n.*159T=
ENST00000477982.2:n.1181A= (FBXL3)
ENST00000485797.2:n.174-8177A= (FBXL3)
ENST00000616833.4:c.*159T= (CLN5)	ENSP00000479547.1:n.*159T=
NM_006493.2:c.*159T= , LRG_692t1:c.*159T= (CLN5)	NP_006484.1:n.*159T=
NM_001366624.1:c.*685T= (CLN5)	NP_001353553.1:n.*685T=
NM_006493.3:c.*159T= (CLN5)	NP_006484.2:n.*159T=
XM_017020538.2:c.644-8177A= (FBXL3)	XP_016876027.1:n.644-8177A=
NM_001366624.2:c.*685T= (CLN5)	NP_001353553.1:n.*685T=
NM_006493.4:c.*159T= (CLN5) MANE Select	NP_006484.2:n.*159T=