Canonical Allele Identifier: CA388315009

Gene: CLN5 FBXL3

Linked Data

• MyVariant Identifiers: chr13:g.77575088C>G (hg19) ; chr13:g.77000953C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000953C>G , CM000675.2:g.77000953C>G	GRCh38
NC_000013.10:g.77575088C>G , CM000675.1:g.77575088C>G	GRCh37
NC_000013.9:g.76473089C>G	NCBI36
NG_009064.1:g.14030C>G , LRG_692:g.14030C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.1061C>G (CLN5) MANE Select	ENSP00000366673.5:p.Thr354Arg
ENST00000616833.6:c.*503C>G (CLN5)	ENSP00000479547.3:n.*503C>G
ENST00000635838.1:c.174+4826C>G
ENST00000635905.1:n.566+4826C>G (CLN5)
ENST00000635915.1:c.1059C>G (CLN5)
ENST00000636183.2:c.1061C>G (CLN5)	ENSP00000490181.2:p.Thr354Arg
ENST00000636525.2:c.565+4826C>G (CLN5)	ENSP00000490078.2:n.565+4826C>G
ENST00000636681.1:c.*752C>G (CLN5)	ENSP00000489922.1:n.*752C>G
ENST00000636705.1:c.897C>G (CLN5)
ENST00000636767.2:c.565+4826C>G (CLN5)	ENSP00000489855.2:n.565+4826C>G
ENST00000636780.2:c.*510C>G (CLN5)	ENSP00000489809.2:n.*510C>G
ENST00000637192.1:c.213+4826C>G
ENST00000637278.1:n.1387C>G (CLN5)
ENST00000637397.2:c.565+4826C>G (CLN5)	ENSP00000490422.2:n.565+4826C>G
ENST00000638101.1:c.169+4826C>G	ENSP00000490535.1:n.169+4826C>G
ENST00000638147.2:c.565+4826C>G	ENSP00000490953.2:n.565+4826C>G
ENST00000377453.7:c.1208C>G (CLN5)	ENSP00000366673.3:p.Thr403Arg
ENST00000477982.2:n.1356G>C (FBXL3)
ENST00000485797.2:n.174-8002G>C (FBXL3)
ENST00000616833.4:c.1061C>G (CLN5)	ENSP00000479547.1:p.Thr354Arg
NM_006493.2:c.1208C>G , LRG_692t1:c.1208C>G (CLN5)	NP_006484.1:p.Thr403Arg
NM_001366624.1:c.*510C>G (CLN5)	NP_001353553.1:n.*510C>G
NM_006493.3:c.1061C>G (CLN5)	NP_006484.2:p.Thr354Arg
XM_017020538.2:c.644-8002G>C (FBXL3)	XP_016876027.1:n.644-8002G>C
NM_001366624.2:c.*510C>G (CLN5)	NP_001353553.1:n.*510C>G
NM_006493.4:c.1061C>G (CLN5) MANE Select	NP_006484.2:p.Thr354Arg