Canonical Allele Identifier: CA2184878975

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209240G= , CM000677.2:g.68209240G=	GRCh38
NC_000015.9:g.68501578G= , CM000677.1:g.68501578G=	GRCh37
NC_000015.8:g.66288632G=	NCBI36
NG_008764.2:g.52972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.665+397C= MANE Select	ENSP00000249806.5:n.665+397C=
ENST00000562767.2:c.84-11612C=	ENSP00000456336.1:n.84-11612C=
ENST00000563917.2:n.507+397C=
ENST00000565471.6:c.206+397C=	ENSP00000457384.1:n.206+397C=
ENST00000635747.1:c.*568+397C=	ENSP00000490627.1:n.*568+397C=
ENST00000636212.1:c.*335+397C=	ENSP00000489851.1:n.*335+397C=
ENST00000636674.1:n.1767+397C=
ENST00000636964.1:n.2193+397C=
ENST00000637054.1:c.198+9296C=	ENSP00000490807.1:n.198+9296C=
ENST00000637329.1:c.634+397C=
ENST00000637450.1:c.*319+397C=	ENSP00000490204.1:n.*319+397C=
ENST00000637494.1:c.377+397C=	ENSP00000490057.1:n.377+397C=
ENST00000637667.1:c.566+397C=	ENSP00000489843.1:n.566+397C=
ENST00000637823.1:c.490+397C=
ENST00000637888.1:c.198+9296C=	ENSP00000490546.1:n.198+9296C=
ENST00000638076.1:c.*268+397C=	ENSP00000490373.1:n.*268+397C=
ENST00000638144.1:n.308+397C=
ENST00000646164.1:c.38+9296C=
ENST00000249806.9:c.665+397C=	ENSP00000249806.5:n.665+397C=
ENST00000538696.5:c.761+397C=	ENSP00000445770.1:n.761+397C=
ENST00000562767.1:c.84-11612C=	ENSP00000456336.1:n.84-11612C=
ENST00000564752.1:c.*49+397C=	ENSP00000457822.1:n.*49+397C=
ENST00000565471.5:c.206+397C=	ENSP00000457384.1:n.206+397C=
ENST00000566347.5:c.476+397C=	ENSP00000457783.1:n.476+397C=
ENST00000567060.5:c.*63+397C=	ENSP00000454818.1:n.*63+397C=
NM_017882.2:c.665+397C=	NP_060352.1:n.665+397C=
XR_931861.1:n.887+397C=
NM_017882.3:c.665+397C= MANE Select	NP_060352.1:n.665+397C=