Canonical Allele Identifier: CA971083235

Gene: CLN6

Linked Data

• dbSNP Id: rs2093225824
• gnomAD v3: 15-68218204-C-CGA
• gnomAD v4: 15-68218204-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218204_68218205insGA , CM000677.2:g.68218204_68218205insGA	GRCh38
NC_000015.9:g.68510542_68510543insGA , CM000677.1:g.68510542_68510543insGA	GRCh37
NC_000015.8:g.66297596_66297597insGA	NCBI36
NG_008764.2:g.44007_44008insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.198+331_198+332insTC MANE Select	ENSP00000249806.5:n.198+331_198+332insTC
ENST00000562767.2:c.83+11297_83+11298insTC	ENSP00000456336.1:n.83+11297_83+11298insTC
ENST00000563917.2:n.41-3817_41-3816insTC
ENST00000565471.6:c.84-8446_84-8445insTC	ENSP00000457384.1:n.84-8446_84-8445insTC
ENST00000569336.2:n.438_439insTC
ENST00000635747.1:c.*101+331_*101+332insTC	ENSP00000490627.1:n.*101+331_*101+332insTC
ENST00000636020.1:n.330+331_330+332insTC
ENST00000636212.1:c.198+331_198+332insTC	ENSP00000489851.1:n.198+331_198+332insTC
ENST00000636314.1:c.84-3817_84-3816insTC	ENSP00000490295.1:n.84-3817_84-3816insTC
ENST00000637054.1:c.198+331_198+332insTC	ENSP00000490807.1:n.198+331_198+332insTC
ENST00000637223.1:c.*101+331_*101+332insTC	ENSP00000490010.1:n.*101+331_*101+332insTC
ENST00000637329.1:c.109+331_109+332insTC
ENST00000637450.1:c.84-3817_84-3816insTC	ENSP00000490204.1:n.84-3817_84-3816insTC
ENST00000637494.1:c.198+331_198+332insTC	ENSP00000490057.1:n.198+331_198+332insTC
ENST00000637667.1:c.198+331_198+332insTC	ENSP00000489843.1:n.198+331_198+332insTC
ENST00000637823.1:c.124+331_124+332insTC
ENST00000637888.1:c.198+331_198+332insTC	ENSP00000490546.1:n.198+331_198+332insTC
ENST00000638076.1:c.198+331_198+332insTC	ENSP00000490373.1:n.198+331_198+332insTC
ENST00000638144.1:n.31-3817_31-3816insTC
ENST00000646164.1:c.38+331_38+332insTC
ENST00000249806.9:c.198+331_198+332insTC	ENSP00000249806.5:n.198+331_198+332insTC
ENST00000538696.5:c.294+331_294+332insTC	ENSP00000445770.1:n.294+331_294+332insTC
ENST00000562767.1:c.83+11297_83+11298insTC	ENSP00000456336.1:n.83+11297_83+11298insTC
ENST00000564752.1:c.198+331_198+332insTC	ENSP00000457822.1:n.198+331_198+332insTC
ENST00000564846.1:n.630+331_630+332insTC
ENST00000565471.5:c.84-8446_84-8445insTC	ENSP00000457384.1:n.84-8446_84-8445insTC
ENST00000566347.5:c.198+331_198+332insTC	ENSP00000457783.1:n.198+331_198+332insTC
ENST00000567060.5:c.198+331_198+332insTC	ENSP00000454818.1:n.198+331_198+332insTC
ENST00000569336.1:n.353+262_353+263insTC
NM_017882.2:c.198+331_198+332insTC	NP_060352.1:n.198+331_198+332insTC
XR_931861.1:n.301+331_301+332insTC
NM_017882.3:c.198+331_198+332insTC MANE Select	NP_060352.1:n.198+331_198+332insTC