Canonical Allele Identifier: CA2575771193

Gene: CLN6

Linked Data

• gnomAD v4: 15-68208438-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208438G>C , CM000677.2:g.68208438G>C	GRCh38
NC_000015.9:g.68500776G>C , CM000677.1:g.68500776G>C	GRCh37
NC_000015.8:g.66287830G>C	NCBI36
NG_008764.2:g.53774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.666-28C>G MANE Select	ENSP00000249806.5:n.666-28C>G
ENST00000562767.2:c.84-10810C>G	ENSP00000456336.1:n.84-10810C>G
ENST00000563917.2:n.508-28C>G
ENST00000565471.6:c.207-28C>G	ENSP00000457384.1:n.207-28C>G
ENST00000635747.1:c.*569-28C>G	ENSP00000490627.1:n.*569-28C>G
ENST00000636212.1:c.*336-28C>G	ENSP00000489851.1:n.*336-28C>G
ENST00000636674.1:n.1768-28C>G
ENST00000636964.1:n.2194-28C>G
ENST00000637054.1:c.198+10098C>G	ENSP00000490807.1:n.198+10098C>G
ENST00000637329.1:c.635-28C>G
ENST00000637450.1:c.*320-28C>G	ENSP00000490204.1:n.*320-28C>G
ENST00000637494.1:c.378-28C>G	ENSP00000490057.1:n.378-28C>G
ENST00000637667.1:c.567-28C>G	ENSP00000489843.1:n.567-28C>G
ENST00000637823.1:c.491-28C>G
ENST00000637888.1:c.198+10098C>G	ENSP00000490546.1:n.198+10098C>G
ENST00000638076.1:c.*269-28C>G	ENSP00000490373.1:n.*269-28C>G
ENST00000638144.1:n.309-28C>G
ENST00000646164.1:c.39-8757C>G
ENST00000249806.9:c.666-28C>G	ENSP00000249806.5:n.666-28C>G
ENST00000538696.5:c.762-28C>G	ENSP00000445770.1:n.762-28C>G
ENST00000562767.1:c.84-10810C>G	ENSP00000456336.1:n.84-10810C>G
ENST00000564752.1:c.*50-28C>G	ENSP00000457822.1:n.*50-28C>G
ENST00000565471.5:c.207-28C>G	ENSP00000457384.1:n.207-28C>G
ENST00000566347.5:c.477-28C>G	ENSP00000457783.1:n.477-28C>G
ENST00000567060.5:c.*64-28C>G	ENSP00000454818.1:n.*64-28C>G
NM_017882.2:c.666-28C>G	NP_060352.1:n.666-28C>G
XR_931861.1:n.888-28C>G
NM_017882.3:c.666-28C>G MANE Select	NP_060352.1:n.666-28C>G