Canonical Allele Identifier: CA484486487

Gene: CLN5 FBXL3

Linked Data

• MyVariant Identifiers: chr13:g.77570081C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76995946C>G , CM000675.2:g.76995946C>G	GRCh38
NC_000013.10:g.77570081C>G , CM000675.1:g.77570081C>G	GRCh37
NC_000013.9:g.76468082C>G	NCBI36
NG_009064.1:g.9023C>G , LRG_692:g.9023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.384C>G (CLN5) MANE Select	ENSP00000366673.5:p.Gly128=
ENST00000485938.4:c.384C>G (CLN5)	ENSP00000482959.3:p.Gly128=
ENST00000616833.6:c.384C>G (CLN5)	ENSP00000479547.3:p.Gly128=
ENST00000635905.1:n.385C>G (CLN5)
ENST00000635915.1:c.382C>G (CLN5)
ENST00000635989.1:n.451C>G (CLN5)
ENST00000636183.2:c.384C>G (CLN5)	ENSP00000490181.2:p.Gly128=
ENST00000636520.1:n.1896C>G (CLN5)
ENST00000636525.2:c.384C>G (CLN5)	ENSP00000490078.2:p.Gly128=
ENST00000636602.1:n.330C>G (CLN5)
ENST00000636681.1:c.*75C>G (CLN5)	ENSP00000489922.1:n.*75C>G
ENST00000636705.1:c.220C>G (CLN5)
ENST00000636767.2:c.384C>G (CLN5)	ENSP00000489855.2:p.Gly128=
ENST00000636780.2:c.384C>G (CLN5)	ENSP00000489809.2:p.Gly128=
ENST00000637192.1:c.32C>G
ENST00000637278.1:n.710C>G (CLN5)
ENST00000637397.2:c.384C>G (CLN5)	ENSP00000490422.2:p.Gly128=
ENST00000637537.2:c.384C>G (CLN5)	ENSP00000489711.2:p.Gly128=
ENST00000638147.2:c.384C>G	ENSP00000490953.2:p.Gly128=
ENST00000377453.7:c.531C>G (CLN5)	ENSP00000366673.3:p.Gly177=
ENST00000485797.2:n.174-2995G>C (FBXL3)
ENST00000485938.2:c.367C>G (CLN5)
ENST00000616833.4:c.384C>G (CLN5)	ENSP00000479547.1:p.Gly128=
NM_006493.2:c.531C>G , LRG_692t1:c.531C>G (CLN5)	NP_006484.1:p.Gly177=
XM_011534917.1:c.531C>G (CLN5)	XP_011533219.1:p.Gly177=
NM_001366624.1:c.384C>G (CLN5)	NP_001353553.1:p.Gly128=
NM_006493.3:c.384C>G (CLN5)	NP_006484.2:p.Gly128=
XM_017020538.2:c.644-2995G>C (FBXL3)	XP_016876027.1:n.644-2995G>C
NM_001366624.2:c.384C>G (CLN5)	NP_001353553.1:p.Gly128=
NM_006493.4:c.384C>G (CLN5) MANE Select	NP_006484.2:p.Gly128=