Canonical Allele Identifier: CA2184872393
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211668G= , CM000677.2:g.68211668G= GRCh38
NC_000015.9:g.68504006G= , CM000677.1:g.68504006G= GRCh37
NC_000015.8:g.66291060G= NCBI36
NG_008764.2:g.50544C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.486+7C= MANE Select ENSP00000249806.5:n.486+7C=
ENST00000562767.2:c.84-14040C= ENSP00000456336.1:n.84-14040C=
ENST00000563917.2:n.328+7C=
ENST00000565471.6:c.84-1909C= ENSP00000457384.1:n.84-1909C=
ENST00000635747.1:c.*389+7C= ENSP00000490627.1:n.*389+7C=
ENST00000636212.1:c.*44C= ENSP00000489851.1:n.*44C=
ENST00000636314.1:c.183-350C= ENSP00000490295.1:n.183-350C=
ENST00000636674.1:n.1476C=
ENST00000636964.1:n.1665C=
ENST00000637054.1:c.198+6868C= ENSP00000490807.1:n.198+6868C=
ENST00000637223.1:c.*201-350C= ENSP00000490010.1:n.*201-350C=
ENST00000637329.1:c.455+7C=
ENST00000637450.1:c.*140+7C= ENSP00000490204.1:n.*140+7C=
ENST00000637494.1:c.199-350C= ENSP00000490057.1:n.199-350C=
ENST00000637667.1:c.387+7C= ENSP00000489843.1:n.387+7C=
ENST00000637823.1:c.224-25C=
ENST00000637888.1:c.198+6868C= ENSP00000490546.1:n.198+6868C=
ENST00000638076.1:c.493C= ENSP00000490373.1:p.Pro165=
ENST00000638144.1:n.130-350C=
ENST00000646164.1:c.38+6868C=
ENST00000249806.9:c.486+7C= ENSP00000249806.5:n.486+7C=
ENST00000538696.5:c.582+7C= ENSP00000445770.1:n.582+7C=
ENST00000562767.1:c.84-14040C= ENSP00000456336.1:n.84-14040C=
ENST00000563917.1:n.274C=
ENST00000564752.1:c.493C= ENSP00000457822.1:p.Pro165=
ENST00000565471.5:c.84-1909C= ENSP00000457384.1:n.84-1909C=
ENST00000566347.5:c.298-350C= ENSP00000457783.1:n.298-350C=
ENST00000567060.5:c.298-1948C= ENSP00000454818.1:n.298-1948C=
NM_017882.2:c.486+7C= NP_060352.1:n.486+7C=
XR_931861.1:n.596C=
NM_017882.3:c.486+7C= MANE Select NP_060352.1:n.486+7C=