Canonical Allele Identifier: CA2184878555

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208739G= , CM000677.2:g.68208739G=	GRCh38
NC_000015.9:g.68501077G= , CM000677.1:g.68501077G=	GRCh37
NC_000015.8:g.66288131G=	NCBI36
NG_008764.2:g.53473C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.666-329C= MANE Select	ENSP00000249806.5:n.666-329C=
ENST00000562767.2:c.84-11111C=	ENSP00000456336.1:n.84-11111C=
ENST00000563917.2:n.508-329C=
ENST00000565471.6:c.207-329C=	ENSP00000457384.1:n.207-329C=
ENST00000635747.1:c.*569-329C=	ENSP00000490627.1:n.*569-329C=
ENST00000636212.1:c.*336-329C=	ENSP00000489851.1:n.*336-329C=
ENST00000636674.1:n.1768-329C=
ENST00000636964.1:n.2194-329C=
ENST00000637054.1:c.198+9797C=	ENSP00000490807.1:n.198+9797C=
ENST00000637329.1:c.635-329C=
ENST00000637450.1:c.*320-329C=	ENSP00000490204.1:n.*320-329C=
ENST00000637494.1:c.378-329C=	ENSP00000490057.1:n.378-329C=
ENST00000637667.1:c.567-329C=	ENSP00000489843.1:n.567-329C=
ENST00000637823.1:c.491-329C=
ENST00000637888.1:c.198+9797C=	ENSP00000490546.1:n.198+9797C=
ENST00000638076.1:c.*269-329C=	ENSP00000490373.1:n.*269-329C=
ENST00000638144.1:n.309-329C=
ENST00000646164.1:c.39-9058C=
ENST00000249806.9:c.666-329C=	ENSP00000249806.5:n.666-329C=
ENST00000538696.5:c.762-329C=	ENSP00000445770.1:n.762-329C=
ENST00000562767.1:c.84-11111C=	ENSP00000456336.1:n.84-11111C=
ENST00000564752.1:c.*50-329C=	ENSP00000457822.1:n.*50-329C=
ENST00000565471.5:c.207-329C=	ENSP00000457384.1:n.207-329C=
ENST00000566347.5:c.477-329C=	ENSP00000457783.1:n.477-329C=
ENST00000567060.5:c.*64-329C=	ENSP00000454818.1:n.*64-329C=
NM_017882.2:c.666-329C=	NP_060352.1:n.666-329C=
XR_931861.1:n.888-329C=
NM_017882.3:c.666-329C= MANE Select	NP_060352.1:n.666-329C=