Canonical Allele Identifier: CA2573142544

Gene: CLN8

Linked Data

• ClinVar Variation Id: 1396473
• ClinVar RCV Id: RCV001902995
• dbSNP Id: rs2129015346

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1780565dup , CM000670.2:g.1780565dup	GRCh38
NC_000008.10:g.1728731dup , CM000670.1:g.1728731dup	GRCh37
NC_000008.9:g.1716138dup	NCBI36
NG_008656.2:g.29788dup , LRG_691:g.29788dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331222.6:c.859dup MANE Select	ENSP00000328182.4:p.Ter287LeuextTer24
ENST00000519254.2:c.859dup	ENSP00000490016.1:p.Ter287LeuextTer24
ENST00000520991.3:c.*270dup	ENSP00000487905.2:n.*270dup
ENST00000635751.1:c.859dup	ENSP00000489694.1:p.Ter287LeuextTer24
ENST00000635773.1:c.496+8968dup
ENST00000635855.1:c.543+8968dup	ENSP00000489726.1:n.543+8968dup
ENST00000635970.1:c.859dup	ENSP00000490439.1:p.Ter287LeuextTer24
ENST00000636175.1:c.343+8968dup
ENST00000636934.1:c.543+8968dup	ENSP00000490218.1:n.543+8968dup
ENST00000637083.1:c.859dup	ENSP00000490235.1:p.Ter287LeuextTer24
ENST00000637156.1:c.859dup	ENSP00000490458.1:p.Ter287LeuextTer24
ENST00000331222.4:c.859dup	ENSP00000328182.4:p.Ter287LeuextTer24
ENST00000519254.1:n.378dup
ENST00000523237.1:n.634dup
NM_018941.3:c.859dup , LRG_691t1:c.859dup	NP_061764.2:p.Ter287LeuextTer24
XM_005266021.3:c.859dup	XP_005266078.1:p.Ter287LeuextTer24
XM_005266022.1:c.859dup	XP_005266079.1:p.Ter287LeuextTer24
XM_005266023.1:c.859dup	XP_005266080.1:p.Ter287LeuextTer24
XM_011534745.1:c.859dup	XP_011533047.1:p.Ter287LeuextTer24
XM_011534746.1:c.859dup	XP_011533048.1:p.Ter287LeuextTer24
XM_005266021.4:c.859dup	XP_005266078.1:p.Ter287LeuextTer24
XM_011534746.2:c.859dup	XP_011533048.1:p.Ter287LeuextTer24
NM_018941.4:c.859dup MANE Select	NP_061764.2:p.Ter287LeuextTer24