Canonical Allele Identifier: CA2804592671

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209950del , CM000677.2:g.68209950del	GRCh38
NC_000015.9:g.68502288del , CM000677.1:g.68502288del	GRCh37
NC_000015.8:g.66289342del	NCBI36
NG_008764.2:g.52262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-191del MANE Select	ENSP00000249806.5:n.543-191del
ENST00000562767.2:c.84-12322del	ENSP00000456336.1:n.84-12322del
ENST00000563917.2:n.385-191del
ENST00000565471.6:c.84-191del	ENSP00000457384.1:n.84-191del
ENST00000635747.1:c.*446-191del	ENSP00000490627.1:n.*446-191del
ENST00000636212.1:c.*213-191del	ENSP00000489851.1:n.*213-191del
ENST00000636314.1:c.239-191del	ENSP00000490295.1:n.239-191del
ENST00000636674.1:n.1645-191del
ENST00000636964.1:n.2071-191del
ENST00000637054.1:c.198+8586del	ENSP00000490807.1:n.198+8586del
ENST00000637223.1:c.*257-191del	ENSP00000490010.1:n.*257-191del
ENST00000637329.1:c.512-191del
ENST00000637450.1:c.*197-191del	ENSP00000490204.1:n.*197-191del
ENST00000637494.1:c.255-191del	ENSP00000490057.1:n.255-191del
ENST00000637667.1:c.444-191del	ENSP00000489843.1:n.444-191del
ENST00000637823.1:c.368-191del
ENST00000637888.1:c.198+8586del	ENSP00000490546.1:n.198+8586del
ENST00000638076.1:c.*146-191del	ENSP00000490373.1:n.*146-191del
ENST00000638144.1:n.186-191del
ENST00000646164.1:c.38+8586del
ENST00000249806.9:c.543-191del	ENSP00000249806.5:n.543-191del
ENST00000538696.5:c.639-191del	ENSP00000445770.1:n.639-191del
ENST00000562767.1:c.84-12322del	ENSP00000456336.1:n.84-12322del
ENST00000563917.1:n.443-191del
ENST00000564752.1:c.569-191del	ENSP00000457822.1:n.569-191del
ENST00000565471.5:c.84-191del	ENSP00000457384.1:n.84-191del
ENST00000566347.5:c.354-191del	ENSP00000457783.1:n.354-191del
ENST00000567060.5:c.298-230del	ENSP00000454818.1:n.298-230del
NM_017882.2:c.543-191del	NP_060352.1:n.543-191del
XR_931861.1:n.765-191del
NM_017882.3:c.543-191del MANE Select	NP_060352.1:n.543-191del