Canonical Allele Identifier: CA2184872794
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211839G= , CM000677.2:g.68211839G= GRCh38
NC_000015.9:g.68504177G= , CM000677.1:g.68504177G= GRCh37
NC_000015.8:g.66291231G= NCBI36
NG_008764.2:g.50373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.322C= MANE Select ENSP00000249806.5:p.Leu108=
ENST00000562767.2:c.84-14211C= ENSP00000456336.1:n.84-14211C=
ENST00000563917.2:n.164C=
ENST00000565471.6:c.84-2080C= ENSP00000457384.1:n.84-2080C=
ENST00000635747.1:c.*225C= ENSP00000490627.1:n.*225C=
ENST00000636212.1:c.298-98C= ENSP00000489851.1:n.298-98C=
ENST00000636314.1:c.183-521C= ENSP00000490295.1:n.183-521C=
ENST00000636674.1:n.1305C=
ENST00000636964.1:n.1494C=
ENST00000637054.1:c.198+6697C= ENSP00000490807.1:n.198+6697C=
ENST00000637223.1:c.*201-521C= ENSP00000490010.1:n.*201-521C=
ENST00000637329.1:c.291C=
ENST00000637450.1:c.207C= ENSP00000490204.1:p.Pro69=
ENST00000637494.1:c.199-521C= ENSP00000490057.1:n.199-521C=
ENST00000637667.1:c.223C= ENSP00000489843.1:p.Leu75=
ENST00000637823.1:c.224-196C=
ENST00000637888.1:c.198+6697C= ENSP00000490546.1:n.198+6697C=
ENST00000638076.1:c.322C= ENSP00000490373.1:p.Leu108=
ENST00000638144.1:n.130-521C=
ENST00000646164.1:c.38+6697C=
ENST00000249806.9:c.322C= ENSP00000249806.5:p.Leu108=
ENST00000538696.5:c.418C= ENSP00000445770.1:p.Leu140=
ENST00000562767.1:c.84-14211C= ENSP00000456336.1:n.84-14211C=
ENST00000563917.1:n.103C=
ENST00000564752.1:c.322C= ENSP00000457822.1:p.Leu108=
ENST00000565471.5:c.84-2080C= ENSP00000457384.1:n.84-2080C=
ENST00000566347.5:c.298-521C= ENSP00000457783.1:n.298-521C=
ENST00000567060.5:c.298-2119C= ENSP00000454818.1:n.298-2119C=
NM_017882.2:c.322C= NP_060352.1:p.Leu108=
XR_931861.1:n.425C=
NM_017882.3:c.322C= MANE Select NP_060352.1:p.Leu108=