Canonical Allele Identifier: CA2103437064

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77001049C= , CM000675.2:g.77001049C=	GRCh38
NC_000013.10:g.77575184C= , CM000675.1:g.77575184C=	GRCh37
NC_000013.9:g.76473185C=	NCBI36
NG_009064.1:g.14126C= , LRG_692:g.14126C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.*80C= (CLN5) MANE Select	ENSP00000366673.5:n.*80C=
ENST00000616833.6:c.*599C= (CLN5)	ENSP00000479547.3:n.*599C=
ENST00000635838.1:c.174+4922C=
ENST00000635905.1:n.566+4922C= (CLN5)
ENST00000635915.1:c.1155C= (CLN5)
ENST00000636183.2:c.*80C= (CLN5)	ENSP00000490181.2:n.*80C=
ENST00000636525.2:c.565+4922C= (CLN5)	ENSP00000490078.2:n.565+4922C=
ENST00000636681.1:c.*848C= (CLN5)	ENSP00000489922.1:n.*848C=
ENST00000636705.1:c.993C= (CLN5)
ENST00000636767.2:c.565+4922C= (CLN5)	ENSP00000489855.2:n.565+4922C=
ENST00000636780.2:c.*606C= (CLN5)	ENSP00000489809.2:n.*606C=
ENST00000637192.1:c.213+4922C=
ENST00000637278.1:n.1483C= (CLN5)
ENST00000637397.2:c.565+4922C= (CLN5)	ENSP00000490422.2:n.565+4922C=
ENST00000638101.1:c.169+4922C=	ENSP00000490535.1:n.169+4922C=
ENST00000638147.2:c.565+4922C=	ENSP00000490953.2:n.565+4922C=
ENST00000377453.7:c.*80C= (CLN5)	ENSP00000366673.3:n.*80C=
ENST00000477982.2:n.1260G= (FBXL3)
ENST00000485797.2:n.174-8098G= (FBXL3)
ENST00000616833.4:c.*80C= (CLN5)	ENSP00000479547.1:n.*80C=
NM_006493.2:c.*80C= , LRG_692t1:c.*80C= (CLN5)	NP_006484.1:n.*80C=
NM_001366624.1:c.*606C= (CLN5)	NP_001353553.1:n.*606C=
NM_006493.3:c.*80C= (CLN5)	NP_006484.2:n.*80C=
XM_017020538.2:c.644-8098G= (FBXL3)	XP_016876027.1:n.644-8098G=
NM_001366624.2:c.*606C= (CLN5)	NP_001353553.1:n.*606C=
NM_006493.4:c.*80C= (CLN5) MANE Select	NP_006484.2:n.*80C=