Canonical Allele Identifier: CA2623297700

Gene: CLN5 FBXL3

Linked Data

• gnomAD v4: 13-76995048-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76995053del , CM000675.2:g.76995053del	GRCh38
NC_000013.10:g.77569188del , CM000675.1:g.77569188del	GRCh37
NC_000013.9:g.76467189del	NCBI36
NG_009064.1:g.8130del , LRG_692:g.8130del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377453.9:c.174-10del (CLN5) MANE Select	ENSP00000366673.5:n.174-10del
ENST00000485938.4:c.174-10del (CLN5)	ENSP00000482959.3:n.174-10del
ENST00000616833.6:c.174-10del (CLN5)	ENSP00000479547.3:n.174-10del
ENST00000635905.1:n.175-10del (CLN5)
ENST00000635915.1:c.113-10del (CLN5)
ENST00000635989.1:n.184-10del (CLN5)
ENST00000636183.2:c.174-10del (CLN5)	ENSP00000490181.2:n.174-10del
ENST00000636520.1:n.1003del (CLN5)
ENST00000636525.2:c.174-10del (CLN5)	ENSP00000490078.2:n.174-10del
ENST00000636681.1:c.-82-10del (CLN5)	ENSP00000489922.1:n.-82-10del
ENST00000636705.1:c.10-10del (CLN5)
ENST00000636767.2:c.174-10del (CLN5)	ENSP00000489855.2:n.174-10del
ENST00000636780.2:c.174-10del (CLN5)	ENSP00000489809.2:n.174-10del
ENST00000637397.2:c.174-10del (CLN5)	ENSP00000490422.2:n.174-10del
ENST00000637537.2:c.174-10del (CLN5)	ENSP00000489711.2:n.174-10del
ENST00000638147.2:c.174-10del	ENSP00000490953.2:n.174-10del
ENST00000377453.7:c.321-10del (CLN5)	ENSP00000366673.3:n.321-10del
ENST00000485797.2:n.174-2098del (FBXL3)
ENST00000485938.2:c.157-10del (CLN5)
ENST00000616833.4:c.174-10del (CLN5)	ENSP00000479547.1:n.174-10del
NM_006493.2:c.321-10del , LRG_692t1:c.321-10del (CLN5)	NP_006484.1:n.321-10del
XM_011534917.1:c.321-10del (CLN5)	XP_011533219.1:n.321-10del
NM_001366624.1:c.174-10del (CLN5)	NP_001353553.1:n.174-10del
NM_006493.3:c.174-10del (CLN5)	NP_006484.2:n.174-10del
XM_017020538.2:c.644-2098del (FBXL3)	XP_016876027.1:n.644-2098del
NM_001366624.2:c.174-10del (CLN5)	NP_001353553.1:n.174-10del
NM_006493.4:c.174-10del (CLN5) MANE Select	NP_006484.2:n.174-10del