Canonical Allele Identifier: CA2623298513

Gene: CLN5 FBXL3

Linked Data

• gnomAD v4: 13-76995858-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76995858G>C , CM000675.2:g.76995858G>C	GRCh38
NC_000013.10:g.77569993G>C , CM000675.1:g.77569993G>C	GRCh37
NC_000013.9:g.76467994G>C	NCBI36
NG_009064.1:g.8935G>C , LRG_692:g.8935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.340-44G>C (CLN5) MANE Select	ENSP00000366673.5:n.340-44G>C
ENST00000485938.4:c.340-44G>C (CLN5)	ENSP00000482959.3:n.340-44G>C
ENST00000616833.6:c.340-44G>C (CLN5)	ENSP00000479547.3:n.340-44G>C
ENST00000635905.1:n.341-44G>C (CLN5)
ENST00000635915.1:c.294G>C (CLN5)
ENST00000635989.1:n.407-44G>C (CLN5)
ENST00000636183.2:c.340-44G>C (CLN5)	ENSP00000490181.2:n.340-44G>C
ENST00000636520.1:n.1808G>C (CLN5)
ENST00000636525.2:c.340-44G>C (CLN5)	ENSP00000490078.2:n.340-44G>C
ENST00000636602.1:n.286-44G>C (CLN5)
ENST00000636681.1:c.*31-44G>C (CLN5)	ENSP00000489922.1:n.*31-44G>C
ENST00000636705.1:c.176-44G>C (CLN5)
ENST00000636767.2:c.340-44G>C (CLN5)	ENSP00000489855.2:n.340-44G>C
ENST00000636780.2:c.340-44G>C (CLN5)	ENSP00000489809.2:n.340-44G>C
ENST00000637278.1:n.622G>C (CLN5)
ENST00000637397.2:c.340-44G>C (CLN5)	ENSP00000490422.2:n.340-44G>C
ENST00000637537.2:c.340-44G>C (CLN5)	ENSP00000489711.2:n.340-44G>C
ENST00000638147.2:c.340-44G>C	ENSP00000490953.2:n.340-44G>C
ENST00000377453.7:c.487-44G>C (CLN5)	ENSP00000366673.3:n.487-44G>C
ENST00000485797.2:n.174-2907C>G (FBXL3)
ENST00000485938.2:c.323-44G>C (CLN5)
ENST00000616833.4:c.340-44G>C (CLN5)	ENSP00000479547.1:n.340-44G>C
NM_006493.2:c.487-44G>C , LRG_692t1:c.487-44G>C (CLN5)	NP_006484.1:n.487-44G>C
XM_011534917.1:c.487-44G>C (CLN5)	XP_011533219.1:n.487-44G>C
NM_001366624.1:c.340-44G>C (CLN5)	NP_001353553.1:n.340-44G>C
NM_006493.3:c.340-44G>C (CLN5)	NP_006484.2:n.340-44G>C
XM_017020538.2:c.644-2907C>G (FBXL3)	XP_016876027.1:n.644-2907C>G
NM_001366624.2:c.340-44G>C (CLN5)	NP_001353553.1:n.340-44G>C
NM_006493.4:c.340-44G>C (CLN5) MANE Select	NP_006484.2:n.340-44G>C