Canonical Allele Identifier: CA2184877953

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208239C= , CM000677.2:g.68208239C=	GRCh38
NC_000015.9:g.68500577C= , CM000677.1:g.68500577C=	GRCh37
NC_000015.8:g.66287631C=	NCBI36
NG_008764.2:g.53973G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.837G= MANE Select	ENSP00000249806.5:p.Trp279=
ENST00000562767.2:c.84-10611G=	ENSP00000456336.1:n.84-10611G=
ENST00000565471.6:c.378G=	ENSP00000457384.1:p.Trp126=
ENST00000635747.1:c.*740G=	ENSP00000490627.1:n.*740G=
ENST00000636212.1:c.*507G=	ENSP00000489851.1:n.*507G=
ENST00000636674.1:n.1939G=
ENST00000636964.1:n.2365G=
ENST00000637054.1:c.198+10297G=	ENSP00000490807.1:n.198+10297G=
ENST00000637329.1:c.806G=
ENST00000637450.1:c.*491G=	ENSP00000490204.1:n.*491G=
ENST00000637494.1:c.549G=	ENSP00000490057.1:p.Trp183=
ENST00000637667.1:c.738G=	ENSP00000489843.1:p.Trp246=
ENST00000637823.1:c.662G=
ENST00000637888.1:c.198+10297G=	ENSP00000490546.1:n.198+10297G=
ENST00000638076.1:c.*440G=	ENSP00000490373.1:n.*440G=
ENST00000638144.1:n.480G=
ENST00000646164.1:c.39-8558G=
ENST00000249806.9:c.837G=	ENSP00000249806.5:p.Trp279=
ENST00000538696.5:c.933G=	ENSP00000445770.1:p.Trp311=
ENST00000562767.1:c.84-10611G=	ENSP00000456336.1:n.84-10611G=
ENST00000565471.5:c.378G=	ENSP00000457384.1:p.Trp126=
ENST00000566347.5:c.648G=	ENSP00000457783.1:p.Trp216=
ENST00000567060.5:c.*235G=	ENSP00000454818.1:n.*235G=
NM_017882.2:c.837G=	NP_060352.1:p.Trp279=
NM_017882.3:c.837G= MANE Select	NP_060352.1:p.Trp279=