Canonical Allele Identifier: CA2184872714

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211812T= , CM000677.2:g.68211812T=	GRCh38
NC_000015.9:g.68504150T= , CM000677.1:g.68504150T=	GRCh37
NC_000015.8:g.66291204T=	NCBI36
NG_008764.2:g.50400A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.349A= MANE Select	ENSP00000249806.5:p.Ile117=
ENST00000562767.2:c.84-14184A=	ENSP00000456336.1:n.84-14184A=
ENST00000563917.2:n.191A=
ENST00000565471.6:c.84-2053A=	ENSP00000457384.1:n.84-2053A=
ENST00000635747.1:c.*252A=	ENSP00000490627.1:n.*252A=
ENST00000636212.1:c.298-71A=	ENSP00000489851.1:n.298-71A=
ENST00000636314.1:c.183-494A=	ENSP00000490295.1:n.183-494A=
ENST00000636674.1:n.1332A=
ENST00000636964.1:n.1521A=
ENST00000637054.1:c.198+6724A=	ENSP00000490807.1:n.198+6724A=
ENST00000637223.1:c.*201-494A=	ENSP00000490010.1:n.*201-494A=
ENST00000637329.1:c.318A=
ENST00000637450.1:c.*3A=	ENSP00000490204.1:n.*3A=
ENST00000637494.1:c.199-494A=	ENSP00000490057.1:n.199-494A=
ENST00000637667.1:c.250A=	ENSP00000489843.1:p.Ile84=
ENST00000637823.1:c.224-169A=
ENST00000637888.1:c.198+6724A=	ENSP00000490546.1:n.198+6724A=
ENST00000638076.1:c.349A=	ENSP00000490373.1:p.Ile117=
ENST00000638144.1:n.130-494A=
ENST00000646164.1:c.38+6724A=
ENST00000249806.9:c.349A=	ENSP00000249806.5:p.Ile117=
ENST00000538696.5:c.445A=	ENSP00000445770.1:p.Ile149=
ENST00000562767.1:c.84-14184A=	ENSP00000456336.1:n.84-14184A=
ENST00000563917.1:n.130A=
ENST00000564752.1:c.349A=	ENSP00000457822.1:p.Ile117=
ENST00000565471.5:c.84-2053A=	ENSP00000457384.1:n.84-2053A=
ENST00000566347.5:c.298-494A=	ENSP00000457783.1:n.298-494A=
ENST00000567060.5:c.298-2092A=	ENSP00000454818.1:n.298-2092A=
NM_017882.2:c.349A=	NP_060352.1:p.Ile117=
XR_931861.1:n.452A=
NM_017882.3:c.349A= MANE Select	NP_060352.1:p.Ile117=