Canonical Allele Identifier: CA1757673134
Gene: CLN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1780323T= , CM000670.2:g.1780323T= GRCh38
NC_000008.10:g.1728489T= , CM000670.1:g.1728489T= GRCh37
NC_000008.9:g.1715896T= NCBI36
NG_008656.2:g.29546T= , LRG_691:g.29546T=

Transcript Alleles

HGVS Amino-acid change
ENST00000331222.6:c.617T= MANE Select ENSP00000328182.4:p.Val206=
ENST00000519254.2:c.617T= ENSP00000490016.1:p.Val206=
ENST00000520991.3:c.*28T= ENSP00000487905.2:n.*28T=
ENST00000635751.1:c.617T= ENSP00000489694.1:p.Val206=
ENST00000635773.1:c.496+8726T=
ENST00000635855.1:c.543+8726T= ENSP00000489726.1:n.543+8726T=
ENST00000635970.1:c.617T= ENSP00000490439.1:p.Val206=
ENST00000636175.1:c.343+8726T=
ENST00000636934.1:c.543+8726T= ENSP00000490218.1:n.543+8726T=
ENST00000637083.1:c.617T= ENSP00000490235.1:p.Val206=
ENST00000637156.1:c.617T= ENSP00000490458.1:p.Val206=
ENST00000331222.4:c.617T= ENSP00000328182.4:p.Val206=
ENST00000519254.1:n.136T=
ENST00000523237.1:n.392T=
NM_018941.3:c.617T= , LRG_691t1:c.617T= NP_061764.2:p.Val206=
XM_005266021.3:c.617T= XP_005266078.1:p.Val206=
XM_005266022.1:c.617T= XP_005266079.1:p.Val206=
XM_005266023.1:c.617T= XP_005266080.1:p.Val206=
XM_011534745.1:c.617T= XP_011533047.1:p.Val206=
XM_011534746.1:c.617T= XP_011533048.1:p.Val206=
XM_005266021.4:c.617T= XP_005266078.1:p.Val206=
XM_011534746.2:c.617T= XP_011533048.1:p.Val206=
NM_018941.4:c.617T= MANE Select NP_061764.2:p.Val206=