Canonical Allele Identifier: CA4599324
Gene: CLN8 HGNC NCBI

Linked Data

dbSNP Id: rs774392784
gnomAD v2: 8-1728502-CA-C
gnomAD v4: 8-1780336-CA-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1780337del , CM000670.2:g.1780337del GRCh38
NC_000008.10:g.1728503del , CM000670.1:g.1728503del GRCh37
NC_000008.9:g.1715910del NCBI36
NG_008656.2:g.29560del , LRG_691:g.29560del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331222.6:c.631del MANE Select ENSP00000328182.4:p.Met211CysfsTer21
ENST00000519254.2:c.631del ENSP00000490016.1:p.Met211CysfsTer21
ENST00000520991.3:c.*42del ENSP00000487905.2:n.*42del
ENST00000635751.1:c.631del ENSP00000489694.1:p.Met211CysfsTer21
ENST00000635773.1:c.496+8740del
ENST00000635855.1:c.543+8740del ENSP00000489726.1:n.543+8740del
ENST00000635970.1:c.631del ENSP00000490439.1:p.Met211CysfsTer21
ENST00000636175.1:c.343+8740del
ENST00000636934.1:c.543+8740del ENSP00000490218.1:n.543+8740del
ENST00000637083.1:c.631del ENSP00000490235.1:p.Met211CysfsTer21
ENST00000637156.1:c.631del ENSP00000490458.1:p.Met211CysfsTer21
ENST00000331222.4:c.631del ENSP00000328182.4:p.Met211CysfsTer21
ENST00000519254.1:n.150del
ENST00000523237.1:n.406del
NM_018941.3:c.631del , LRG_691t1:c.631del NP_061764.2:p.Met211CysfsTer21
XM_005266021.3:c.631del XP_005266078.1:p.Met211CysfsTer21
XM_005266022.1:c.631del XP_005266079.1:p.Met211CysfsTer21
XM_005266023.1:c.631del XP_005266080.1:p.Met211CysfsTer21
XM_011534745.1:c.631del XP_011533047.1:p.Met211CysfsTer21
XM_011534746.1:c.631del XP_011533048.1:p.Met211CysfsTer21
XM_005266021.4:c.631del XP_005266078.1:p.Met211CysfsTer21
XM_011534746.2:c.631del XP_011533048.1:p.Met211CysfsTer21
NM_018941.4:c.631del MANE Select NP_061764.2:p.Met211CysfsTer21