Canonical Allele Identifier: CA2103435927

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000723_77000724delinsGC , CM000675.2:g.77000723_77000724delinsGC	GRCh38
NC_000013.10:g.77574858_77574859delinsGC , CM000675.1:g.77574858_77574859delinsGC	GRCh37
NC_000013.9:g.76472859_76472860delinsGC	NCBI36
NG_009064.1:g.13800_13801delinsGC , LRG_692:g.13800_13801delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.831_832delinsGC (CLN5) MANE Select	ENSP00000366673.5:p.Gly277=
ENST00000616833.6:c.*273_*274delinsGC (CLN5)	ENSP00000479547.3:n.*273_*274delinsGC
ENST00000635838.1:c.174+4596_174+4597delinsGC
ENST00000635905.1:n.566+4596_566+4597delinsGC (CLN5)
ENST00000635915.1:c.829_830delinsGC (CLN5)
ENST00000636183.2:c.831_832delinsGC (CLN5)	ENSP00000490181.2:p.Gly277=
ENST00000636525.2:c.565+4596_565+4597delinsGC (CLN5)	ENSP00000490078.2:n.565+4596_565+4597delinsGC
ENST00000636681.1:c.*522_*523delinsGC (CLN5)	ENSP00000489922.1:n.*522_*523delinsGC
ENST00000636705.1:c.667_668delinsGC (CLN5)
ENST00000636767.2:c.565+4596_565+4597delinsGC (CLN5)	ENSP00000489855.2:n.565+4596_565+4597delinsGC
ENST00000636780.2:c.*280_*281delinsGC (CLN5)	ENSP00000489809.2:n.*280_*281delinsGC
ENST00000637192.1:c.213+4596_213+4597delinsGC
ENST00000637278.1:n.1157_1158delinsGC (CLN5)
ENST00000637397.2:c.565+4596_565+4597delinsGC (CLN5)	ENSP00000490422.2:n.565+4596_565+4597delinsGC
ENST00000638101.1:c.169+4596_169+4597delinsGC	ENSP00000490535.1:n.169+4596_169+4597delinsGC
ENST00000638147.2:c.565+4596_565+4597delinsGC	ENSP00000490953.2:n.565+4596_565+4597delinsGC
ENST00000377453.7:c.978_979delinsGC (CLN5)	ENSP00000366673.3:p.Gly326=
ENST00000477982.2:n.1585_1586delinsGC (FBXL3)
ENST00000485797.2:n.174-7773_174-7772delinsGC (FBXL3)
ENST00000616833.4:c.831_832delinsGC (CLN5)	ENSP00000479547.1:p.Gly277=
NM_006493.2:c.978_979delinsGC , LRG_692t1:c.978_979delinsGC (CLN5)	NP_006484.1:p.Gly326=
XM_011534917.1:c.*280_*281delinsGC (CLN5)	XP_011533219.1:n.*280_*281delinsGC
NM_001366624.1:c.*280_*281delinsGC (CLN5)	NP_001353553.1:n.*280_*281delinsGC
NM_006493.3:c.831_832delinsGC (CLN5)	NP_006484.2:p.Gly277=
XM_017020538.2:c.644-7773_644-7772delinsGC (FBXL3)	XP_016876027.1:n.644-7773_644-7772delinsGC
NM_001366624.2:c.*280_*281delinsGC (CLN5)	NP_001353553.1:n.*280_*281delinsGC
NM_006493.4:c.831_832delinsGC (CLN5) MANE Select	NP_006484.2:p.Gly277=