Canonical Allele Identifier: CA2184872318

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211635C= , CM000677.2:g.68211635C=	GRCh38
NC_000015.9:g.68503973C= , CM000677.1:g.68503973C=	GRCh37
NC_000015.8:g.66291027C=	NCBI36
NG_008764.2:g.50577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+40G= MANE Select	ENSP00000249806.5:n.486+40G=
ENST00000562767.2:c.84-14007G=	ENSP00000456336.1:n.84-14007G=
ENST00000563917.2:n.328+40G=
ENST00000565471.6:c.84-1876G=	ENSP00000457384.1:n.84-1876G=
ENST00000635747.1:c.*389+40G=	ENSP00000490627.1:n.*389+40G=
ENST00000636212.1:c.*77G=	ENSP00000489851.1:n.*77G=
ENST00000636314.1:c.183-317G=	ENSP00000490295.1:n.183-317G=
ENST00000636674.1:n.1509G=
ENST00000636964.1:n.1698G=
ENST00000637054.1:c.198+6901G=	ENSP00000490807.1:n.198+6901G=
ENST00000637223.1:c.*201-317G=	ENSP00000490010.1:n.*201-317G=
ENST00000637329.1:c.455+40G=
ENST00000637450.1:c.*140+40G=	ENSP00000490204.1:n.*140+40G=
ENST00000637494.1:c.199-317G=	ENSP00000490057.1:n.199-317G=
ENST00000637667.1:c.387+40G=	ENSP00000489843.1:n.387+40G=
ENST00000637823.1:c.232G=
ENST00000637888.1:c.198+6901G=	ENSP00000490546.1:n.198+6901G=
ENST00000638076.1:c.*10G=	ENSP00000490373.1:n.*10G=
ENST00000638144.1:n.130-317G=
ENST00000646164.1:c.38+6901G=
ENST00000249806.9:c.486+40G=	ENSP00000249806.5:n.486+40G=
ENST00000538696.5:c.582+40G=	ENSP00000445770.1:n.582+40G=
ENST00000562767.1:c.84-14007G=	ENSP00000456336.1:n.84-14007G=
ENST00000563917.1:n.307G=
ENST00000564752.1:c.512+14G=	ENSP00000457822.1:n.512+14G=
ENST00000565471.5:c.84-1876G=	ENSP00000457384.1:n.84-1876G=
ENST00000566347.5:c.298-317G=	ENSP00000457783.1:n.298-317G=
ENST00000567060.5:c.298-1915G=	ENSP00000454818.1:n.298-1915G=
NM_017882.2:c.486+40G=	NP_060352.1:n.486+40G=
XR_931861.1:n.629G=
NM_017882.3:c.486+40G= MANE Select	NP_060352.1:n.486+40G=