Canonical Allele Identifier: CA2184872788
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211837C= , CM000677.2:g.68211837C= GRCh38
NC_000015.9:g.68504175C= , CM000677.1:g.68504175C= GRCh37
NC_000015.8:g.66291229C= NCBI36
NG_008764.2:g.50375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.324G= MANE Select ENSP00000249806.5:p.Leu108=
ENST00000562767.2:c.84-14209G= ENSP00000456336.1:n.84-14209G=
ENST00000563917.2:n.166G=
ENST00000565471.6:c.84-2078G= ENSP00000457384.1:n.84-2078G=
ENST00000635747.1:c.*227G= ENSP00000490627.1:n.*227G=
ENST00000636212.1:c.298-96G= ENSP00000489851.1:n.298-96G=
ENST00000636314.1:c.183-519G= ENSP00000490295.1:n.183-519G=
ENST00000636674.1:n.1307G=
ENST00000636964.1:n.1496G=
ENST00000637054.1:c.198+6699G= ENSP00000490807.1:n.198+6699G=
ENST00000637223.1:c.*201-519G= ENSP00000490010.1:n.*201-519G=
ENST00000637329.1:c.293G=
ENST00000637450.1:c.209G= ENSP00000490204.1:p.Cys70=
ENST00000637494.1:c.199-519G= ENSP00000490057.1:n.199-519G=
ENST00000637667.1:c.225G= ENSP00000489843.1:p.Leu75=
ENST00000637823.1:c.224-194G=
ENST00000637888.1:c.198+6699G= ENSP00000490546.1:n.198+6699G=
ENST00000638076.1:c.324G= ENSP00000490373.1:p.Leu108=
ENST00000638144.1:n.130-519G=
ENST00000646164.1:c.38+6699G=
ENST00000249806.9:c.324G= ENSP00000249806.5:p.Leu108=
ENST00000538696.5:c.420G= ENSP00000445770.1:p.Leu140=
ENST00000562767.1:c.84-14209G= ENSP00000456336.1:n.84-14209G=
ENST00000563917.1:n.105G=
ENST00000564752.1:c.324G= ENSP00000457822.1:p.Leu108=
ENST00000565471.5:c.84-2078G= ENSP00000457384.1:n.84-2078G=
ENST00000566347.5:c.298-519G= ENSP00000457783.1:n.298-519G=
ENST00000567060.5:c.298-2117G= ENSP00000454818.1:n.298-2117G=
NM_017882.2:c.324G= NP_060352.1:p.Leu108=
XR_931861.1:n.427G=
NM_017882.3:c.324G= MANE Select NP_060352.1:p.Leu108=