Canonical Allele Identifier: CA2184872829

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211849G= , CM000677.2:g.68211849G=	GRCh38
NC_000015.9:g.68504187G= , CM000677.1:g.68504187G=	GRCh37
NC_000015.8:g.66291241G=	NCBI36
NG_008764.2:g.50363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.312C= MANE Select	ENSP00000249806.5:p.Ser104=
ENST00000562767.2:c.84-14221C=	ENSP00000456336.1:n.84-14221C=
ENST00000563917.2:n.154C=
ENST00000565471.6:c.84-2090C=	ENSP00000457384.1:n.84-2090C=
ENST00000635747.1:c.*215C=	ENSP00000490627.1:n.*215C=
ENST00000636212.1:c.298-108C=	ENSP00000489851.1:n.298-108C=
ENST00000636314.1:c.183-531C=	ENSP00000490295.1:n.183-531C=
ENST00000636674.1:n.1295C=
ENST00000636964.1:n.1484C=
ENST00000637054.1:c.198+6687C=	ENSP00000490807.1:n.198+6687C=
ENST00000637223.1:c.*201-531C=	ENSP00000490010.1:n.*201-531C=
ENST00000637329.1:c.281C=
ENST00000637450.1:c.197C=	ENSP00000490204.1:p.Pro66=
ENST00000637494.1:c.199-531C=	ENSP00000490057.1:n.199-531C=
ENST00000637667.1:c.213C=	ENSP00000489843.1:p.Ser71=
ENST00000637823.1:c.224-206C=
ENST00000637888.1:c.198+6687C=	ENSP00000490546.1:n.198+6687C=
ENST00000638076.1:c.312C=	ENSP00000490373.1:p.Ser104=
ENST00000638144.1:n.130-531C=
ENST00000646164.1:c.38+6687C=
ENST00000249806.9:c.312C=	ENSP00000249806.5:p.Ser104=
ENST00000538696.5:c.408C=	ENSP00000445770.1:p.Ser136=
ENST00000562767.1:c.84-14221C=	ENSP00000456336.1:n.84-14221C=
ENST00000563917.1:n.93C=
ENST00000564752.1:c.312C=	ENSP00000457822.1:p.Ser104=
ENST00000565471.5:c.84-2090C=	ENSP00000457384.1:n.84-2090C=
ENST00000566347.5:c.298-531C=	ENSP00000457783.1:n.298-531C=
ENST00000567060.5:c.298-2129C=	ENSP00000454818.1:n.298-2129C=
NM_017882.2:c.312C=	NP_060352.1:p.Ser104=
XR_931861.1:n.415C=
NM_017882.3:c.312C= MANE Select	NP_060352.1:p.Ser104=