Canonical Allele Identifier: CA1757673339

Gene: CLN8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1780689_1780693delinsTACTA , CM000670.2:g.1780689_1780693delinsTACTA	GRCh38
NC_000008.10:g.1728855_1728859delinsTACTA , CM000670.1:g.1728855_1728859delinsTACTA	GRCh37
NC_000008.9:g.1716262_1716266delinsTACTA	NCBI36
NG_008656.2:g.29912_29916delinsTACTA , LRG_691:g.29912_29916delinsTACTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331222.6:c.*122_*126delinsTACTA MANE Select	ENSP00000328182.4:n.*122_*126delinsTACTA
ENST00000519254.2:c.*122_*126delinsTACTA	ENSP00000490016.1:n.*122_*126delinsTACTA
ENST00000520991.3:c.*394_*398delinsTACTA	ENSP00000487905.2:n.*394_*398delinsTACTA
ENST00000635751.1:c.*122_*126delinsTACTA	ENSP00000489694.1:n.*122_*126delinsTACTA
ENST00000635773.1:c.496+9092_496+9096delinsTACTA
ENST00000635855.1:c.543+9092_543+9096delinsTACTA	ENSP00000489726.1:n.543+9092_543+9096delinsTACTA
ENST00000635970.1:c.*122_*126delinsTACTA	ENSP00000490439.1:n.*122_*126delinsTACTA
ENST00000636175.1:c.343+9092_343+9096delinsTACTA
ENST00000636934.1:c.543+9092_543+9096delinsTACTA	ENSP00000490218.1:n.543+9092_543+9096delinsTACTA
ENST00000637083.1:c.*122_*126delinsTACTA	ENSP00000490235.1:n.*122_*126delinsTACTA
ENST00000637156.1:c.*122_*126delinsTACTA	ENSP00000490458.1:n.*122_*126delinsTACTA
ENST00000331222.4:c.*122_*126delinsTACTA	ENSP00000328182.4:n.*122_*126delinsTACTA
ENST00000519254.1:n.502_506delinsTACTA
ENST00000523237.1:n.758_762delinsTACTA
NM_018941.3:c.*122_*126delinsTACTA , LRG_691t1:c.*122_*126delinsTACTA	NP_061764.2:n.*122_*126delinsTACTA
XM_005266021.3:c.*122_*126delinsTACTA	XP_005266078.1:n.*122_*126delinsTACTA
XM_005266022.1:c.*122_*126delinsTACTA	XP_005266079.1:n.*122_*126delinsTACTA
XM_005266023.1:c.*122_*126delinsTACTA	XP_005266080.1:n.*122_*126delinsTACTA
XM_011534745.1:c.*122_*126delinsTACTA	XP_011533047.1:n.*122_*126delinsTACTA
XM_011534746.1:c.*122_*126delinsTACTA	XP_011533048.1:n.*122_*126delinsTACTA
XM_005266021.4:c.*122_*126delinsTACTA	XP_005266078.1:n.*122_*126delinsTACTA
XM_011534746.2:c.*122_*126delinsTACTA	XP_011533048.1:n.*122_*126delinsTACTA
NM_018941.4:c.*122_*126delinsTACTA MANE Select	NP_061764.2:n.*122_*126delinsTACTA