Canonical Allele Identifier: CA2184872825
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211847G= , CM000677.2:g.68211847G= GRCh38
NC_000015.9:g.68504185G= , CM000677.1:g.68504185G= GRCh37
NC_000015.8:g.66291239G= NCBI36
NG_008764.2:g.50365C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.314C= MANE Select ENSP00000249806.5:p.Pro105=
ENST00000562767.2:c.84-14219C= ENSP00000456336.1:n.84-14219C=
ENST00000563917.2:n.156C=
ENST00000565471.6:c.84-2088C= ENSP00000457384.1:n.84-2088C=
ENST00000635747.1:c.*217C= ENSP00000490627.1:n.*217C=
ENST00000636212.1:c.298-106C= ENSP00000489851.1:n.298-106C=
ENST00000636314.1:c.183-529C= ENSP00000490295.1:n.183-529C=
ENST00000636674.1:n.1297C=
ENST00000636964.1:n.1486C=
ENST00000637054.1:c.198+6689C= ENSP00000490807.1:n.198+6689C=
ENST00000637223.1:c.*201-529C= ENSP00000490010.1:n.*201-529C=
ENST00000637329.1:c.283C=
ENST00000637450.1:c.199C= ENSP00000490204.1:p.Pro67=
ENST00000637494.1:c.199-529C= ENSP00000490057.1:n.199-529C=
ENST00000637667.1:c.215C= ENSP00000489843.1:p.Pro72=
ENST00000637823.1:c.224-204C=
ENST00000637888.1:c.198+6689C= ENSP00000490546.1:n.198+6689C=
ENST00000638076.1:c.314C= ENSP00000490373.1:p.Pro105=
ENST00000638144.1:n.130-529C=
ENST00000646164.1:c.38+6689C=
ENST00000249806.9:c.314C= ENSP00000249806.5:p.Pro105=
ENST00000538696.5:c.410C= ENSP00000445770.1:p.Pro137=
ENST00000562767.1:c.84-14219C= ENSP00000456336.1:n.84-14219C=
ENST00000563917.1:n.95C=
ENST00000564752.1:c.314C= ENSP00000457822.1:p.Pro105=
ENST00000565471.5:c.84-2088C= ENSP00000457384.1:n.84-2088C=
ENST00000566347.5:c.298-529C= ENSP00000457783.1:n.298-529C=
ENST00000567060.5:c.298-2127C= ENSP00000454818.1:n.298-2127C=
NM_017882.2:c.314C= NP_060352.1:p.Pro105=
XR_931861.1:n.417C=
NM_017882.3:c.314C= MANE Select NP_060352.1:p.Pro105=