Canonical Allele Identifier: CA2184872364

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211658G= , CM000677.2:g.68211658G=	GRCh38
NC_000015.9:g.68503996G= , CM000677.1:g.68503996G=	GRCh37
NC_000015.8:g.66291050G=	NCBI36
NG_008764.2:g.50554C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+17C= MANE Select	ENSP00000249806.5:n.486+17C=
ENST00000562767.2:c.84-14030C=	ENSP00000456336.1:n.84-14030C=
ENST00000563917.2:n.328+17C=
ENST00000565471.6:c.84-1899C=	ENSP00000457384.1:n.84-1899C=
ENST00000635747.1:c.*389+17C=	ENSP00000490627.1:n.*389+17C=
ENST00000636212.1:c.*54C=	ENSP00000489851.1:n.*54C=
ENST00000636314.1:c.183-340C=	ENSP00000490295.1:n.183-340C=
ENST00000636674.1:n.1486C=
ENST00000636964.1:n.1675C=
ENST00000637054.1:c.198+6878C=	ENSP00000490807.1:n.198+6878C=
ENST00000637223.1:c.*201-340C=	ENSP00000490010.1:n.*201-340C=
ENST00000637329.1:c.455+17C=
ENST00000637450.1:c.*140+17C=	ENSP00000490204.1:n.*140+17C=
ENST00000637494.1:c.199-340C=	ENSP00000490057.1:n.199-340C=
ENST00000637667.1:c.387+17C=	ENSP00000489843.1:n.387+17C=
ENST00000637823.1:c.224-15C=
ENST00000637888.1:c.198+6878C=	ENSP00000490546.1:n.198+6878C=
ENST00000638076.1:c.503C=	ENSP00000490373.1:p.Ala168=
ENST00000638144.1:n.130-340C=
ENST00000646164.1:c.38+6878C=
ENST00000249806.9:c.486+17C=	ENSP00000249806.5:n.486+17C=
ENST00000538696.5:c.582+17C=	ENSP00000445770.1:n.582+17C=
ENST00000562767.1:c.84-14030C=	ENSP00000456336.1:n.84-14030C=
ENST00000563917.1:n.284C=
ENST00000564752.1:c.503C=	ENSP00000457822.1:p.Ala168=
ENST00000565471.5:c.84-1899C=	ENSP00000457384.1:n.84-1899C=
ENST00000566347.5:c.298-340C=	ENSP00000457783.1:n.298-340C=
ENST00000567060.5:c.298-1938C=	ENSP00000454818.1:n.298-1938C=
NM_017882.2:c.486+17C=	NP_060352.1:n.486+17C=
XR_931861.1:n.606C=
NM_017882.3:c.486+17C= MANE Select	NP_060352.1:n.486+17C=