Canonical Allele Identifier: CA2184878200

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218266_68218267delinsAG , CM000677.2:g.68218266_68218267delinsAG	GRCh38
NC_000015.9:g.68510604_68510605delinsAG , CM000677.1:g.68510604_68510605delinsAG	GRCh37
NC_000015.8:g.66297658_66297659delinsAG	NCBI36
NG_008764.2:g.43945_43946delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.198+269_198+270delinsCT MANE Select	ENSP00000249806.5:n.198+269_198+270delinsCT
ENST00000562767.2:c.83+11235_83+11236delinsCT	ENSP00000456336.1:n.83+11235_83+11236delinsCT
ENST00000563917.2:n.41-3879_41-3878delinsCT
ENST00000565471.6:c.84-8508_84-8507delinsCT	ENSP00000457384.1:n.84-8508_84-8507delinsCT
ENST00000569336.2:n.376_377delinsCT
ENST00000635747.1:c.*101+269_*101+270delinsCT	ENSP00000490627.1:n.*101+269_*101+270delinsCT
ENST00000636020.1:n.330+269_330+270delinsCT
ENST00000636212.1:c.198+269_198+270delinsCT	ENSP00000489851.1:n.198+269_198+270delinsCT
ENST00000636314.1:c.84-3879_84-3878delinsCT	ENSP00000490295.1:n.84-3879_84-3878delinsCT
ENST00000637054.1:c.198+269_198+270delinsCT	ENSP00000490807.1:n.198+269_198+270delinsCT
ENST00000637223.1:c.*101+269_*101+270delinsCT	ENSP00000490010.1:n.*101+269_*101+270delinsCT
ENST00000637329.1:c.109+269_109+270delinsCT
ENST00000637450.1:c.84-3879_84-3878delinsCT	ENSP00000490204.1:n.84-3879_84-3878delinsCT
ENST00000637494.1:c.198+269_198+270delinsCT	ENSP00000490057.1:n.198+269_198+270delinsCT
ENST00000637667.1:c.198+269_198+270delinsCT	ENSP00000489843.1:n.198+269_198+270delinsCT
ENST00000637823.1:c.124+269_124+270delinsCT
ENST00000637888.1:c.198+269_198+270delinsCT	ENSP00000490546.1:n.198+269_198+270delinsCT
ENST00000638076.1:c.198+269_198+270delinsCT	ENSP00000490373.1:n.198+269_198+270delinsCT
ENST00000638144.1:n.31-3879_31-3878delinsCT
ENST00000646164.1:c.38+269_38+270delinsCT
ENST00000249806.9:c.198+269_198+270delinsCT	ENSP00000249806.5:n.198+269_198+270delinsCT
ENST00000538696.5:c.294+269_294+270delinsCT	ENSP00000445770.1:n.294+269_294+270delinsCT
ENST00000562767.1:c.83+11235_83+11236delinsCT	ENSP00000456336.1:n.83+11235_83+11236delinsCT
ENST00000564752.1:c.198+269_198+270delinsCT	ENSP00000457822.1:n.198+269_198+270delinsCT
ENST00000564846.1:n.630+269_630+270delinsCT
ENST00000565471.5:c.84-8508_84-8507delinsCT	ENSP00000457384.1:n.84-8508_84-8507delinsCT
ENST00000566347.5:c.198+269_198+270delinsCT	ENSP00000457783.1:n.198+269_198+270delinsCT
ENST00000567060.5:c.198+269_198+270delinsCT	ENSP00000454818.1:n.198+269_198+270delinsCT
ENST00000569336.1:n.353+200_353+201delinsCT
NM_017882.2:c.198+269_198+270delinsCT	NP_060352.1:n.198+269_198+270delinsCT
XR_931861.1:n.301+269_301+270delinsCT
NM_017882.3:c.198+269_198+270delinsCT MANE Select	NP_060352.1:n.198+269_198+270delinsCT