Canonical Allele Identifier: CA2184872666
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211798G= , CM000677.2:g.68211798G= GRCh38
NC_000015.9:g.68504136G= , CM000677.1:g.68504136G= GRCh37
NC_000015.8:g.66291190G= NCBI36
NG_008764.2:g.50414C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.363C= MANE Select ENSP00000249806.5:p.Ile121=
ENST00000562767.2:c.84-14170C= ENSP00000456336.1:n.84-14170C=
ENST00000563917.2:n.205C=
ENST00000565471.6:c.84-2039C= ENSP00000457384.1:n.84-2039C=
ENST00000635747.1:c.*266C= ENSP00000490627.1:n.*266C=
ENST00000636212.1:c.298-57C= ENSP00000489851.1:n.298-57C=
ENST00000636314.1:c.183-480C= ENSP00000490295.1:n.183-480C=
ENST00000636674.1:n.1346C=
ENST00000636964.1:n.1535C=
ENST00000637054.1:c.198+6738C= ENSP00000490807.1:n.198+6738C=
ENST00000637223.1:c.*201-480C= ENSP00000490010.1:n.*201-480C=
ENST00000637329.1:c.332C=
ENST00000637450.1:c.*17C= ENSP00000490204.1:n.*17C=
ENST00000637494.1:c.199-480C= ENSP00000490057.1:n.199-480C=
ENST00000637667.1:c.264C= ENSP00000489843.1:p.Ile88=
ENST00000637823.1:c.224-155C=
ENST00000637888.1:c.198+6738C= ENSP00000490546.1:n.198+6738C=
ENST00000638076.1:c.363C= ENSP00000490373.1:p.Ile121=
ENST00000638144.1:n.130-480C=
ENST00000646164.1:c.38+6738C=
ENST00000249806.9:c.363C= ENSP00000249806.5:p.Ile121=
ENST00000538696.5:c.459C= ENSP00000445770.1:p.Ile153=
ENST00000562767.1:c.84-14170C= ENSP00000456336.1:n.84-14170C=
ENST00000563917.1:n.144C=
ENST00000564752.1:c.363C= ENSP00000457822.1:p.Ile121=
ENST00000565471.5:c.84-2039C= ENSP00000457384.1:n.84-2039C=
ENST00000566347.5:c.298-480C= ENSP00000457783.1:n.298-480C=
ENST00000567060.5:c.298-2078C= ENSP00000454818.1:n.298-2078C=
NM_017882.2:c.363C= NP_060352.1:p.Ile121=
XR_931861.1:n.466C=
NM_017882.3:c.363C= MANE Select NP_060352.1:p.Ile121=