Canonical Allele Identifier: CA2695199765

Gene: CLN5 FBXL3

Linked Data

• ClinVar Variation Id: 2680828
• ClinVar RCV Id: RCV003468468

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000609dup , CM000675.2:g.77000609dup	GRCh38
NC_000013.10:g.77574744dup , CM000675.1:g.77574744dup	GRCh37
NC_000013.9:g.76472745dup	NCBI36
NG_009064.1:g.13686dup , LRG_692:g.13686dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.717dup (CLN5) MANE Select	ENSP00000366673.5:p.Asn240Ter
ENST00000616833.6:c.*159dup (CLN5)	ENSP00000479547.3:n.*159dup
ENST00000635838.1:c.174+4482dup
ENST00000635905.1:n.566+4482dup (CLN5)
ENST00000635915.1:c.715dup (CLN5)
ENST00000636183.2:c.717dup (CLN5)	ENSP00000490181.2:p.Asn240Ter
ENST00000636525.2:c.565+4482dup (CLN5)	ENSP00000490078.2:n.565+4482dup
ENST00000636681.1:c.*408dup (CLN5)	ENSP00000489922.1:n.*408dup
ENST00000636705.1:c.553dup (CLN5)
ENST00000636767.2:c.565+4482dup (CLN5)	ENSP00000489855.2:n.565+4482dup
ENST00000636780.2:c.*166dup (CLN5)	ENSP00000489809.2:n.*166dup
ENST00000637192.1:c.213+4482dup
ENST00000637278.1:n.1043dup (CLN5)
ENST00000637397.2:c.565+4482dup (CLN5)	ENSP00000490422.2:n.565+4482dup
ENST00000638101.1:c.169+4482dup	ENSP00000490535.1:n.169+4482dup
ENST00000638147.2:c.565+4482dup	ENSP00000490953.2:n.565+4482dup
ENST00000377453.7:c.864dup (CLN5)	ENSP00000366673.3:p.Asn289Ter
ENST00000477982.2:n.1702dup (FBXL3)
ENST00000485797.2:n.174-7656dup (FBXL3)
ENST00000616833.4:c.717dup (CLN5)	ENSP00000479547.1:p.Asn240Ter
NM_006493.2:c.864dup , LRG_692t1:c.864dup (CLN5)	NP_006484.1:p.Asn289Ter
XM_011534917.1:c.*166dup (CLN5)	XP_011533219.1:n.*166dup
NM_001366624.1:c.*166dup (CLN5)	NP_001353553.1:n.*166dup
NM_006493.3:c.717dup (CLN5)	NP_006484.2:p.Asn240Ter
XM_017020538.2:c.644-7656dup (FBXL3)	XP_016876027.1:n.644-7656dup
NM_001366624.2:c.*166dup (CLN5)	NP_001353553.1:n.*166dup
NM_006493.4:c.717dup (CLN5) MANE Select	NP_006484.2:p.Asn240Ter