Canonical Allele Identifier: CA2184879600

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209706G= , CM000677.2:g.68209706G=	GRCh38
NC_000015.9:g.68502044G= , CM000677.1:g.68502044G=	GRCh37
NC_000015.8:g.66289098G=	NCBI36
NG_008764.2:g.52506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.596C= MANE Select	ENSP00000249806.5:p.Ala199=
ENST00000562767.2:c.84-12078C=	ENSP00000456336.1:n.84-12078C=
ENST00000563917.2:n.438C=
ENST00000565471.6:c.137C=	ENSP00000457384.1:p.Ala46=
ENST00000635747.1:c.*499C=	ENSP00000490627.1:n.*499C=
ENST00000636212.1:c.*266C=	ENSP00000489851.1:n.*266C=
ENST00000636314.1:c.292C=	ENSP00000490295.1:p.Pro98=
ENST00000636674.1:n.1698C=
ENST00000636964.1:n.2124C=
ENST00000637054.1:c.198+8830C=	ENSP00000490807.1:n.198+8830C=
ENST00000637223.1:c.*310C=	ENSP00000490010.1:n.*310C=
ENST00000637329.1:c.565C=
ENST00000637450.1:c.*250C=	ENSP00000490204.1:n.*250C=
ENST00000637494.1:c.308C=	ENSP00000490057.1:p.Ala103=
ENST00000637667.1:c.497C=	ENSP00000489843.1:p.Ala166=
ENST00000637823.1:c.421C=
ENST00000637888.1:c.198+8830C=	ENSP00000490546.1:n.198+8830C=
ENST00000638076.1:c.*199C=	ENSP00000490373.1:n.*199C=
ENST00000638144.1:n.239C=
ENST00000646164.1:c.38+8830C=
ENST00000249806.9:c.596C=	ENSP00000249806.5:p.Ala199=
ENST00000538696.5:c.692C=	ENSP00000445770.1:p.Ala231=
ENST00000562767.1:c.84-12078C=	ENSP00000456336.1:n.84-12078C=
ENST00000563917.1:n.496C=
ENST00000564752.1:c.622C=	ENSP00000457822.1:p.Pro208=
ENST00000565471.5:c.137C=	ENSP00000457384.1:p.Ala46=
ENST00000566347.5:c.407C=	ENSP00000457783.1:p.Ala136=
ENST00000567060.5:c.312C=	ENSP00000454818.1:p.Cys104=
NM_017882.2:c.596C=	NP_060352.1:p.Ala199=
XR_931861.1:n.818C=
NM_017882.3:c.596C= MANE Select	NP_060352.1:p.Ala199=