Canonical Allele Identifier: CA388312257

Gene: CLN5 FBXL3

Linked Data

• ClinVar Variation Id: 650446
• ClinVar RCV Id: RCV000805601
• dbSNP Id: rs1593914834
• MyVariant Identifiers: chr13:g.77574729T>G (hg19) ; chr13:g.77000594T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000594T>G , CM000675.2:g.77000594T>G	GRCh38
NC_000013.10:g.77574729T>G , CM000675.1:g.77574729T>G	GRCh37
NC_000013.9:g.76472730T>G	NCBI36
NG_009064.1:g.13671T>G , LRG_692:g.13671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.702T>G (CLN5) MANE Select	ENSP00000366673.5:p.Phe234Leu
ENST00000616833.6:c.*144T>G (CLN5)	ENSP00000479547.3:n.*144T>G
ENST00000635838.1:c.174+4467T>G
ENST00000635905.1:n.566+4467T>G (CLN5)
ENST00000635915.1:c.700T>G (CLN5)
ENST00000636183.2:c.702T>G (CLN5)	ENSP00000490181.2:p.Phe234Leu
ENST00000636525.2:c.565+4467T>G (CLN5)	ENSP00000490078.2:n.565+4467T>G
ENST00000636681.1:c.*393T>G (CLN5)	ENSP00000489922.1:n.*393T>G
ENST00000636705.1:c.538T>G (CLN5)
ENST00000636767.2:c.565+4467T>G (CLN5)	ENSP00000489855.2:n.565+4467T>G
ENST00000636780.2:c.*151T>G (CLN5)	ENSP00000489809.2:n.*151T>G
ENST00000637192.1:c.213+4467T>G
ENST00000637278.1:n.1028T>G (CLN5)
ENST00000637397.2:c.565+4467T>G (CLN5)	ENSP00000490422.2:n.565+4467T>G
ENST00000638101.1:c.169+4467T>G	ENSP00000490535.1:n.169+4467T>G
ENST00000638147.2:c.565+4467T>G	ENSP00000490953.2:n.565+4467T>G
ENST00000377453.7:c.849T>G (CLN5)	ENSP00000366673.3:p.Phe283Leu
ENST00000477982.2:n.1715A>C (FBXL3)
ENST00000485797.2:n.174-7643A>C (FBXL3)
ENST00000616833.4:c.702T>G (CLN5)	ENSP00000479547.1:p.Phe234Leu
NM_006493.2:c.849T>G , LRG_692t1:c.849T>G (CLN5)	NP_006484.1:p.Phe283Leu
XM_011534917.1:c.*151T>G (CLN5)	XP_011533219.1:n.*151T>G
NM_001366624.1:c.*151T>G (CLN5)	NP_001353553.1:n.*151T>G
NM_006493.3:c.702T>G (CLN5)	NP_006484.2:p.Phe234Leu
XM_017020538.2:c.644-7643A>C (FBXL3)	XP_016876027.1:n.644-7643A>C
NM_001366624.2:c.*151T>G (CLN5)	NP_001353553.1:n.*151T>G
NM_006493.4:c.702T>G (CLN5) MANE Select	NP_006484.2:p.Phe234Leu