Canonical Allele Identifier: CA2184872896

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211877T= , CM000677.2:g.68211877T=	GRCh38
NC_000015.9:g.68504215T= , CM000677.1:g.68504215T=	GRCh37
NC_000015.8:g.66291269T=	NCBI36
NG_008764.2:g.50335A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-14A= MANE Select	ENSP00000249806.5:n.298-14A=
ENST00000562767.2:c.84-14249A=	ENSP00000456336.1:n.84-14249A=
ENST00000563917.2:n.140-14A=
ENST00000565471.6:c.84-2118A=	ENSP00000457384.1:n.84-2118A=
ENST00000635747.1:c.*201-14A=	ENSP00000490627.1:n.*201-14A=
ENST00000636212.1:c.298-136A=	ENSP00000489851.1:n.298-136A=
ENST00000636314.1:c.183-559A=	ENSP00000490295.1:n.183-559A=
ENST00000636674.1:n.1267A=
ENST00000636964.1:n.1456A=
ENST00000637054.1:c.198+6659A=	ENSP00000490807.1:n.198+6659A=
ENST00000637223.1:c.*201-559A=	ENSP00000490010.1:n.*201-559A=
ENST00000637329.1:c.253A=
ENST00000637450.1:c.183-14A=	ENSP00000490204.1:n.183-14A=
ENST00000637494.1:c.199-559A=	ENSP00000490057.1:n.199-559A=
ENST00000637667.1:c.199-14A=	ENSP00000489843.1:n.199-14A=
ENST00000637823.1:c.224-234A=
ENST00000637888.1:c.198+6659A=	ENSP00000490546.1:n.198+6659A=
ENST00000638076.1:c.298-14A=	ENSP00000490373.1:n.298-14A=
ENST00000638144.1:n.130-559A=
ENST00000646164.1:c.38+6659A=
ENST00000249806.9:c.298-14A=	ENSP00000249806.5:n.298-14A=
ENST00000538696.5:c.394-14A=	ENSP00000445770.1:n.394-14A=
ENST00000562767.1:c.84-14249A=	ENSP00000456336.1:n.84-14249A=
ENST00000563917.1:n.79-14A=
ENST00000564752.1:c.298-14A=	ENSP00000457822.1:n.298-14A=
ENST00000565471.5:c.84-2118A=	ENSP00000457384.1:n.84-2118A=
ENST00000566347.5:c.298-559A=	ENSP00000457783.1:n.298-559A=
ENST00000567060.5:c.298-2157A=	ENSP00000454818.1:n.298-2157A=
NM_017882.2:c.298-14A=	NP_060352.1:n.298-14A=
XR_931861.1:n.401-14A=
NM_017882.3:c.298-14A= MANE Select	NP_060352.1:n.298-14A=