Canonical Allele Identifier: CA274121
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 188917
dbSNP Id: rs746645358
gnomAD v2: 8-1728581-G-A
gnomAD v3: 8-1780415-G-A
gnomAD v4: 8-1780415-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1780415G>A , CM000670.2:g.1780415G>A GRCh38
NC_000008.10:g.1728581G>A , CM000670.1:g.1728581G>A GRCh37
NC_000008.9:g.1715988G>A NCBI36
NG_008656.2:g.29638G>A , LRG_691:g.29638G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331222.6:c.709G>A MANE Select ENSP00000328182.4:p.Gly237Arg
ENST00000519254.2:c.709G>A ENSP00000490016.1:p.Gly237Arg
ENST00000520991.3:c.*120G>A ENSP00000487905.2:n.*120G>A
ENST00000635751.1:c.709G>A ENSP00000489694.1:p.Gly237Arg
ENST00000635773.1:c.496+8818G>A
ENST00000635855.1:c.543+8818G>A ENSP00000489726.1:n.543+8818G>A
ENST00000635970.1:c.709G>A ENSP00000490439.1:p.Gly237Arg
ENST00000636175.1:c.343+8818G>A
ENST00000636934.1:c.543+8818G>A ENSP00000490218.1:n.543+8818G>A
ENST00000637083.1:c.709G>A ENSP00000490235.1:p.Gly237Arg
ENST00000637156.1:c.709G>A ENSP00000490458.1:p.Gly237Arg
ENST00000331222.4:c.709G>A ENSP00000328182.4:p.Gly237Arg
ENST00000519254.1:n.228G>A
ENST00000523237.1:n.484G>A
NM_018941.3:c.709G>A , LRG_691t1:c.709G>A NP_061764.2:p.Gly237Arg
XM_005266021.3:c.709G>A XP_005266078.1:p.Gly237Arg
XM_005266022.1:c.709G>A XP_005266079.1:p.Gly237Arg
XM_005266023.1:c.709G>A XP_005266080.1:p.Gly237Arg
XM_011534745.1:c.709G>A XP_011533047.1:p.Gly237Arg
XM_011534746.1:c.709G>A XP_011533048.1:p.Gly237Arg
XM_005266021.4:c.709G>A XP_005266078.1:p.Gly237Arg
XM_011534746.2:c.709G>A XP_011533048.1:p.Gly237Arg
NM_018941.4:c.709G>A MANE Select NP_061764.2:p.Gly237Arg