Canonical Allele Identifier: CA2103437252

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77001149C= , CM000675.2:g.77001149C=	GRCh38
NC_000013.10:g.77575284C= , CM000675.1:g.77575284C=	GRCh37
NC_000013.9:g.76473285C=	NCBI36
NG_009064.1:g.14226C= , LRG_692:g.14226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.*180C= (CLN5) MANE Select	ENSP00000366673.5:n.*180C=
ENST00000616833.6:c.*699C= (CLN5)	ENSP00000479547.3:n.*699C=
ENST00000635838.1:c.174+5022C=
ENST00000635905.1:n.566+5022C= (CLN5)
ENST00000635915.1:c.1255C= (CLN5)
ENST00000636183.2:c.*180C= (CLN5)	ENSP00000490181.2:n.*180C=
ENST00000636525.2:c.565+5022C= (CLN5)	ENSP00000490078.2:n.565+5022C=
ENST00000636681.1:c.*948C= (CLN5)	ENSP00000489922.1:n.*948C=
ENST00000636705.1:c.1093C= (CLN5)
ENST00000636767.2:c.565+5022C= (CLN5)	ENSP00000489855.2:n.565+5022C=
ENST00000636780.2:c.*706C= (CLN5)	ENSP00000489809.2:n.*706C=
ENST00000637192.1:c.213+5022C=
ENST00000637278.1:n.1583C= (CLN5)
ENST00000637397.2:c.565+5022C= (CLN5)	ENSP00000490422.2:n.565+5022C=
ENST00000638101.1:c.169+5022C=	ENSP00000490535.1:n.169+5022C=
ENST00000638147.2:c.565+5022C=	ENSP00000490953.2:n.565+5022C=
ENST00000377453.7:c.*180C= (CLN5)	ENSP00000366673.3:n.*180C=
ENST00000477982.2:n.1160G= (FBXL3)
ENST00000485797.2:n.174-8198G= (FBXL3)
ENST00000616833.4:c.*180C= (CLN5)	ENSP00000479547.1:n.*180C=
NM_006493.2:c.*180C= , LRG_692t1:c.*180C= (CLN5)	NP_006484.1:n.*180C=
NM_001366624.1:c.*706C= (CLN5)	NP_001353553.1:n.*706C=
NM_006493.3:c.*180C= (CLN5)	NP_006484.2:n.*180C=
XM_017020538.2:c.644-8198G= (FBXL3)	XP_016876027.1:n.644-8198G=
NM_001366624.2:c.*706C= (CLN5)	NP_001353553.1:n.*706C=
NM_006493.4:c.*180C= (CLN5) MANE Select	NP_006484.2:n.*180C=