Canonical Allele Identifier: CA2184877666

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208127T= , CM000677.2:g.68208127T=	GRCh38
NC_000015.9:g.68500465T= , CM000677.1:g.68500465T=	GRCh37
NC_000015.8:g.66287519T=	NCBI36
NG_008764.2:g.54085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.*13A= MANE Select	ENSP00000249806.5:n.*13A=
ENST00000562767.2:c.84-10499A=	ENSP00000456336.1:n.84-10499A=
ENST00000565471.6:c.*13A=	ENSP00000457384.1:n.*13A=
ENST00000635747.1:c.*852A=	ENSP00000490627.1:n.*852A=
ENST00000636964.1:n.2477A=
ENST00000637054.1:c.198+10409A=	ENSP00000490807.1:n.198+10409A=
ENST00000637329.1:c.918A=
ENST00000637494.1:c.*13A=	ENSP00000490057.1:n.*13A=
ENST00000637888.1:c.198+10409A=	ENSP00000490546.1:n.198+10409A=
ENST00000638076.1:c.*552A=	ENSP00000490373.1:n.*552A=
ENST00000646164.1:c.39-8446A=
ENST00000249806.9:c.*13A=	ENSP00000249806.5:n.*13A=
ENST00000538696.5:c.*13A=	ENSP00000445770.1:n.*13A=
ENST00000562767.1:c.84-10499A=	ENSP00000456336.1:n.84-10499A=
ENST00000565471.5:c.*13A=	ENSP00000457384.1:n.*13A=
ENST00000566347.5:c.*13A=	ENSP00000457783.1:n.*13A=
ENST00000567060.5:c.*347A=	ENSP00000454818.1:n.*347A=
NM_017882.2:c.*13A=	NP_060352.1:n.*13A=
NM_017882.3:c.*13A= MANE Select	NP_060352.1:n.*13A=