Canonical Allele Identifier: CA4599380

Gene: CLN8

Linked Data

• ClinVar Variation Id: 1218523
• ClinVar RCV Id: RCV001592365
• dbSNP Id: rs200904267
• ExAC: 8:1728758 G / A
• gnomAD v2: 8-1728758-G-A
• gnomAD v3: 8-1780592-G-A
• gnomAD v4: 8-1780592-G-A
• MyVariant Identifiers: chr8:g.1728758G>A (hg19) ; chr8:g.1780592G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1780592G>A , CM000670.2:g.1780592G>A	GRCh38
NC_000008.10:g.1728758G>A , CM000670.1:g.1728758G>A	GRCh37
NC_000008.9:g.1716165G>A	NCBI36
NG_008656.2:g.29815G>A , LRG_691:g.29815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331222.6:c.*25G>A MANE Select	ENSP00000328182.4:n.*25G>A
ENST00000519254.2:c.*25G>A	ENSP00000490016.1:n.*25G>A
ENST00000520991.3:c.*297G>A	ENSP00000487905.2:n.*297G>A
ENST00000635751.1:c.*25G>A	ENSP00000489694.1:n.*25G>A
ENST00000635773.1:c.496+8995G>A
ENST00000635855.1:c.543+8995G>A	ENSP00000489726.1:n.543+8995G>A
ENST00000635970.1:c.*25G>A	ENSP00000490439.1:n.*25G>A
ENST00000636175.1:c.343+8995G>A
ENST00000636934.1:c.543+8995G>A	ENSP00000490218.1:n.543+8995G>A
ENST00000637083.1:c.*25G>A	ENSP00000490235.1:n.*25G>A
ENST00000637156.1:c.*25G>A	ENSP00000490458.1:n.*25G>A
ENST00000331222.4:c.*25G>A	ENSP00000328182.4:n.*25G>A
ENST00000519254.1:n.405G>A
ENST00000523237.1:n.661G>A
NM_018941.3:c.*25G>A , LRG_691t1:c.*25G>A	NP_061764.2:n.*25G>A
XM_005266021.3:c.*25G>A	XP_005266078.1:n.*25G>A
XM_005266022.1:c.*25G>A	XP_005266079.1:n.*25G>A
XM_005266023.1:c.*25G>A	XP_005266080.1:n.*25G>A
XM_011534745.1:c.*25G>A	XP_011533047.1:n.*25G>A
XM_011534746.1:c.*25G>A	XP_011533048.1:n.*25G>A
XM_005266021.4:c.*25G>A	XP_005266078.1:n.*25G>A
XM_011534746.2:c.*25G>A	XP_011533048.1:n.*25G>A
NM_018941.4:c.*25G>A MANE Select	NP_061764.2:n.*25G>A