Canonical Allele Identifier: CA2184878121

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218143_68218144delinsGT , CM000677.2:g.68218143_68218144delinsGT	GRCh38
NC_000015.9:g.68510481_68510482delinsGT , CM000677.1:g.68510481_68510482delinsGT	GRCh37
NC_000015.8:g.66297535_66297536delinsGT	NCBI36
NG_008764.2:g.44068_44069delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.198+392_198+393delinsAC MANE Select	ENSP00000249806.5:n.198+392_198+393delinsAC
ENST00000562767.2:c.83+11358_83+11359delinsAC	ENSP00000456336.1:n.83+11358_83+11359delinsAC
ENST00000563917.2:n.41-3756_41-3755delinsAC
ENST00000565471.6:c.84-8385_84-8384delinsAC	ENSP00000457384.1:n.84-8385_84-8384delinsAC
ENST00000569336.2:n.499_500delinsAC
ENST00000635747.1:c.*101+392_*101+393delinsAC	ENSP00000490627.1:n.*101+392_*101+393delinsAC
ENST00000636020.1:n.330+392_330+393delinsAC
ENST00000636212.1:c.198+392_198+393delinsAC	ENSP00000489851.1:n.198+392_198+393delinsAC
ENST00000636314.1:c.84-3756_84-3755delinsAC	ENSP00000490295.1:n.84-3756_84-3755delinsAC
ENST00000637054.1:c.198+392_198+393delinsAC	ENSP00000490807.1:n.198+392_198+393delinsAC
ENST00000637223.1:c.*101+392_*101+393delinsAC	ENSP00000490010.1:n.*101+392_*101+393delinsAC
ENST00000637329.1:c.109+392_109+393delinsAC
ENST00000637450.1:c.84-3756_84-3755delinsAC	ENSP00000490204.1:n.84-3756_84-3755delinsAC
ENST00000637494.1:c.198+392_198+393delinsAC	ENSP00000490057.1:n.198+392_198+393delinsAC
ENST00000637667.1:c.198+392_198+393delinsAC	ENSP00000489843.1:n.198+392_198+393delinsAC
ENST00000637823.1:c.124+392_124+393delinsAC
ENST00000637888.1:c.198+392_198+393delinsAC	ENSP00000490546.1:n.198+392_198+393delinsAC
ENST00000638076.1:c.198+392_198+393delinsAC	ENSP00000490373.1:n.198+392_198+393delinsAC
ENST00000638144.1:n.31-3756_31-3755delinsAC
ENST00000646164.1:c.38+392_38+393delinsAC
ENST00000249806.9:c.198+392_198+393delinsAC	ENSP00000249806.5:n.198+392_198+393delinsAC
ENST00000538696.5:c.294+392_294+393delinsAC	ENSP00000445770.1:n.294+392_294+393delinsAC
ENST00000562767.1:c.83+11358_83+11359delinsAC	ENSP00000456336.1:n.83+11358_83+11359delinsAC
ENST00000564752.1:c.198+392_198+393delinsAC	ENSP00000457822.1:n.198+392_198+393delinsAC
ENST00000564846.1:n.630+392_630+393delinsAC
ENST00000565471.5:c.84-8385_84-8384delinsAC	ENSP00000457384.1:n.84-8385_84-8384delinsAC
ENST00000566347.5:c.198+392_198+393delinsAC	ENSP00000457783.1:n.198+392_198+393delinsAC
ENST00000567060.5:c.198+392_198+393delinsAC	ENSP00000454818.1:n.198+392_198+393delinsAC
ENST00000569336.1:n.353+323_353+324delinsAC
NM_017882.2:c.198+392_198+393delinsAC	NP_060352.1:n.198+392_198+393delinsAC
XR_931861.1:n.301+392_301+393delinsAC
NM_017882.3:c.198+392_198+393delinsAC MANE Select	NP_060352.1:n.198+392_198+393delinsAC