Canonical Allele Identifier: CA2103434918

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000460A= , CM000675.2:g.77000460A=	GRCh38
NC_000013.10:g.77574595A= , CM000675.1:g.77574595A=	GRCh37
NC_000013.9:g.76472596A=	NCBI36
NG_009064.1:g.13537A= , LRG_692:g.13537A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.568A= (CLN5) MANE Select	ENSP00000366673.5:p.Asn190=
ENST00000616833.6:c.*10A= (CLN5)	ENSP00000479547.3:n.*10A=
ENST00000635838.1:c.174+4333A=
ENST00000635905.1:n.566+4333A= (CLN5)
ENST00000635915.1:c.566A= (CLN5)
ENST00000636183.2:c.568A= (CLN5)	ENSP00000490181.2:p.Asn190=
ENST00000636525.2:c.565+4333A= (CLN5)	ENSP00000490078.2:n.565+4333A=
ENST00000636681.1:c.*259A= (CLN5)	ENSP00000489922.1:n.*259A=
ENST00000636705.1:c.404A= (CLN5)
ENST00000636767.2:c.565+4333A= (CLN5)	ENSP00000489855.2:n.565+4333A=
ENST00000636780.2:c.*17A= (CLN5)	ENSP00000489809.2:n.*17A=
ENST00000637192.1:c.213+4333A=
ENST00000637278.1:n.894A= (CLN5)
ENST00000637397.2:c.565+4333A= (CLN5)	ENSP00000490422.2:n.565+4333A=
ENST00000638101.1:c.169+4333A=	ENSP00000490535.1:n.169+4333A=
ENST00000638147.2:c.565+4333A=	ENSP00000490953.2:n.565+4333A=
ENST00000377453.7:c.715A= (CLN5)	ENSP00000366673.3:p.Asn239=
ENST00000477982.2:n.1849T= (FBXL3)
ENST00000485797.2:n.174-7509T= (FBXL3)
ENST00000616833.4:c.568A= (CLN5)	ENSP00000479547.1:p.Asn190=
NM_006493.2:c.715A= , LRG_692t1:c.715A= (CLN5)	NP_006484.1:p.Asn239=
XM_011534917.1:c.*17A= (CLN5)	XP_011533219.1:n.*17A=
NM_001366624.1:c.*17A= (CLN5)	NP_001353553.1:n.*17A=
NM_006493.3:c.568A= (CLN5)	NP_006484.2:p.Asn190=
XM_017020538.2:c.644-7509T= (FBXL3)	XP_016876027.1:n.644-7509T=
NM_001366624.2:c.*17A= (CLN5)	NP_001353553.1:n.*17A=
NM_006493.4:c.568A= (CLN5) MANE Select	NP_006484.2:p.Asn190=