Canonical Allele Identifier: CA2184872959

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211924C= , CM000677.2:g.68211924C=	GRCh38
NC_000015.9:g.68504262C= , CM000677.1:g.68504262C=	GRCh37
NC_000015.8:g.66291316C=	NCBI36
NG_008764.2:g.50288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-61G= MANE Select	ENSP00000249806.5:n.298-61G=
ENST00000562767.2:c.84-14296G=	ENSP00000456336.1:n.84-14296G=
ENST00000563917.2:n.140-61G=
ENST00000565471.6:c.84-2165G=	ENSP00000457384.1:n.84-2165G=
ENST00000635747.1:c.*201-61G=	ENSP00000490627.1:n.*201-61G=
ENST00000636212.1:c.298-183G=	ENSP00000489851.1:n.298-183G=
ENST00000636314.1:c.183-606G=	ENSP00000490295.1:n.183-606G=
ENST00000636674.1:n.1220G=
ENST00000636964.1:n.1409G=
ENST00000637054.1:c.198+6612G=	ENSP00000490807.1:n.198+6612G=
ENST00000637223.1:c.*201-606G=	ENSP00000490010.1:n.*201-606G=
ENST00000637329.1:c.209-3G=
ENST00000637450.1:c.183-61G=	ENSP00000490204.1:n.183-61G=
ENST00000637494.1:c.199-606G=	ENSP00000490057.1:n.199-606G=
ENST00000637667.1:c.199-61G=	ENSP00000489843.1:n.199-61G=
ENST00000637823.1:c.224-281G=
ENST00000637888.1:c.198+6612G=	ENSP00000490546.1:n.198+6612G=
ENST00000638076.1:c.298-61G=	ENSP00000490373.1:n.298-61G=
ENST00000638144.1:n.130-606G=
ENST00000646164.1:c.38+6612G=
ENST00000249806.9:c.298-61G=	ENSP00000249806.5:n.298-61G=
ENST00000538696.5:c.394-61G=	ENSP00000445770.1:n.394-61G=
ENST00000562767.1:c.84-14296G=	ENSP00000456336.1:n.84-14296G=
ENST00000563917.1:n.79-61G=
ENST00000564752.1:c.298-61G=	ENSP00000457822.1:n.298-61G=
ENST00000565471.5:c.84-2165G=	ENSP00000457384.1:n.84-2165G=
ENST00000566347.5:c.298-606G=	ENSP00000457783.1:n.298-606G=
ENST00000567060.5:c.298-2204G=	ENSP00000454818.1:n.298-2204G=
NM_017882.2:c.298-61G=	NP_060352.1:n.298-61G=
XR_931861.1:n.401-61G=
NM_017882.3:c.298-61G= MANE Select	NP_060352.1:n.298-61G=