Canonical Allele Identifier: CA2103422990

Gene: CLN5 FBXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76995175C= , CM000675.2:g.76995175C=	GRCh38
NC_000013.10:g.77569310C= , CM000675.1:g.77569310C=	GRCh37
NC_000013.9:g.76467311C=	NCBI36
NG_009064.1:g.8252C= , LRG_692:g.8252C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006493.4:c.286C= (CLN5) MANE Select	NP_006484.2:p.Arg96=
ENST00000377453.9:c.286C= (CLN5) MANE Select	ENSP00000366673.5:p.Arg96=
NM_001366624.1:c.286C= (CLN5)	NP_001353553.1:p.Arg96=
NM_001366624.2:c.286C= (CLN5)	NP_001353553.1:p.Arg96=
NM_006493.2:c.433C= , LRG_692t1:c.433C= (CLN5)	NP_006484.1:p.Arg145=
NM_006493.3:c.286C= (CLN5)	NP_006484.2:p.Arg96=
ENST00000377453.7:c.433C= (CLN5)	ENSP00000366673.3:p.Arg145=
ENST00000485797.2:n.174-2224G= (FBXL3)
ENST00000485938.2:c.269C= (CLN5)
ENST00000485938.4:c.286C= (CLN5)	ENSP00000482959.3:p.Arg96=
ENST00000616833.4:c.286C= (CLN5)	ENSP00000479547.1:p.Arg96=
ENST00000616833.6:c.286C= (CLN5)	ENSP00000479547.3:p.Arg96=
ENST00000635905.1:n.287C= (CLN5)
ENST00000635915.1:c.225C= (CLN5)
ENST00000635989.1:n.296C= (CLN5)
ENST00000636183.2:c.286C= (CLN5)	ENSP00000490181.2:p.Arg96=
ENST00000636520.1:n.1125C= (CLN5)
ENST00000636525.2:c.286C= (CLN5)	ENSP00000490078.2:p.Arg96=
ENST00000636681.1:c.31C= (CLN5)	ENSP00000489922.1:p.Arg11=
ENST00000636705.1:c.122C= (CLN5)
ENST00000636767.2:c.286C= (CLN5)	ENSP00000489855.2:p.Arg96=
ENST00000636780.2:c.286C= (CLN5)	ENSP00000489809.2:p.Arg96=
ENST00000637397.2:c.286C= (CLN5)	ENSP00000490422.2:p.Arg96=
ENST00000637537.2:c.286C= (CLN5)	ENSP00000489711.2:p.Arg96=
ENST00000638147.2:c.286C=	ENSP00000490953.2:p.Arg96=
XM_011534917.1:c.433C= (CLN5)	XP_011533219.1:p.Arg145=
XM_017020538.2:c.644-2224G= (FBXL3)	XP_016876027.1:n.644-2224G=