Canonical Allele Identifier: CA2804592477

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209280G>T , CM000677.2:g.68209280G>T	GRCh38
NC_000015.9:g.68501618G>T , CM000677.1:g.68501618G>T	GRCh37
NC_000015.8:g.66288672G>T	NCBI36
NG_008764.2:g.52932C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.665+357C>A MANE Select	ENSP00000249806.5:n.665+357C>A
ENST00000562767.2:c.84-11652C>A	ENSP00000456336.1:n.84-11652C>A
ENST00000563917.2:n.507+357C>A
ENST00000565471.6:c.206+357C>A	ENSP00000457384.1:n.206+357C>A
ENST00000635747.1:c.*568+357C>A	ENSP00000490627.1:n.*568+357C>A
ENST00000636212.1:c.*335+357C>A	ENSP00000489851.1:n.*335+357C>A
ENST00000636674.1:n.1767+357C>A
ENST00000636964.1:n.2193+357C>A
ENST00000637054.1:c.198+9256C>A	ENSP00000490807.1:n.198+9256C>A
ENST00000637329.1:c.634+357C>A
ENST00000637450.1:c.*319+357C>A	ENSP00000490204.1:n.*319+357C>A
ENST00000637494.1:c.377+357C>A	ENSP00000490057.1:n.377+357C>A
ENST00000637667.1:c.566+357C>A	ENSP00000489843.1:n.566+357C>A
ENST00000637823.1:c.490+357C>A
ENST00000637888.1:c.198+9256C>A	ENSP00000490546.1:n.198+9256C>A
ENST00000638076.1:c.*268+357C>A	ENSP00000490373.1:n.*268+357C>A
ENST00000638144.1:n.308+357C>A
ENST00000646164.1:c.38+9256C>A
ENST00000249806.9:c.665+357C>A	ENSP00000249806.5:n.665+357C>A
ENST00000538696.5:c.761+357C>A	ENSP00000445770.1:n.761+357C>A
ENST00000562767.1:c.84-11652C>A	ENSP00000456336.1:n.84-11652C>A
ENST00000564752.1:c.*49+357C>A	ENSP00000457822.1:n.*49+357C>A
ENST00000565471.5:c.206+357C>A	ENSP00000457384.1:n.206+357C>A
ENST00000566347.5:c.476+357C>A	ENSP00000457783.1:n.476+357C>A
ENST00000567060.5:c.*63+357C>A	ENSP00000454818.1:n.*63+357C>A
NM_017882.2:c.665+357C>A	NP_060352.1:n.665+357C>A
XR_931861.1:n.887+357C>A
NM_017882.3:c.665+357C>A MANE Select	NP_060352.1:n.665+357C>A